rs398124146

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs398124146(C;T)

Make rs398124146(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

3738617

Gene

CREBBP

is a	snp
is	mentioned by
dbSNP	rs398124146
dbSNP (classic)	rs398124146
ClinGen	rs398124146
ebi	rs398124146
HLI	rs398124146
Exac	rs398124146
Gnomad	rs398124146
Varsome	rs398124146
LitVar	rs398124146
Map	rs398124146
PheGenI	rs398124146
Biobank	rs398124146
1000 genomes	rs398124146
hgdp	rs398124146
ensembl	rs398124146
geneview	rs398124146
scholar	rs398124146
google	rs398124146
pharmgkb	rs398124146
gwascentral	rs398124146
openSNP	rs398124146
23andMe	rs398124146
SNPshot	rs398124146
SNPdbe	rs398124146
MSV3d	rs398124146
GWAS Ctlg	rs398124146

Max Magnitude

0

ClinVar
Risk	rs398124146(G;G) rs398124146(T;T)
Alt	rs398124146(G;G) rs398124146(T;T)
Reference	Rs398124146(C;C)
Significance	Probable-Pathogenic
Disease	not specified Medulloblastoma Uterine cervical neoplasms Colorectal Neoplasms Adenocarcinoma of stomach Glioblastoma Hepatocellular carcinoma Adenoid cystic carcinoma Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Squamous cell carcinoma of lung Malignant melanoma of skin
Variation	info
Gene	CREBBP
CLNDBN	not specified Medulloblastoma Uterine cervical neoplasms Colorectal Neoplasms Adenocarcinoma of stomach Glioblastoma Hepatocellular carcinoma Adenoid cystic carcinoma Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Squamous cell carcinoma of lung Malignant melanoma of skin
Reversed	1
HGVS	NC_000016.9:g.3788618G>A; NC_000016.9:g.3788618G>C
CLNSRC
CLNACC	RCV000081052.4, RCV000418574.1, RCV000423556.1, RCV000425760.1, RCV000426447.1, RCV000426681.1, RCV000433226.1, RCV000434703.1, RCV000436055.1, RCV000441267.1, RCV000442404.1, RCV000443206.1, RCV000419312.1, RCV000422245.1, RCV000423470.1, RCV000428778.1, RCV000430036.1, RCV000431113.1, RCV000432952.1, RCV000438307.1, RCV000439458.1, RCV000440692.1, RCV000442935.1,