rs770248150

Orientation

plus

Stabilized

plus

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

Make rs770248150(A;A)

Make rs770248150(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

25225713

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs770248150
dbSNP (classic)	rs770248150
ClinGen	rs770248150
ebi	rs770248150
HLI	rs770248150
Exac	rs770248150
Gnomad	rs770248150
Varsome	rs770248150
LitVar	rs770248150
Map	rs770248150
PheGenI	rs770248150
Biobank	rs770248150
1000 genomes	rs770248150
hgdp	rs770248150
ensembl	rs770248150
geneview	rs770248150
scholar	rs770248150
google	rs770248150
pharmgkb	rs770248150
gwascentral	rs770248150
openSNP	rs770248150
23andMe	rs770248150
SNPshot	rs770248150
SNPdbe	rs770248150
MSV3d	rs770248150
GWAS Ctlg	rs770248150

Max Magnitude

0

ClinVar
Risk	rs770248150(A;A) rs770248150(G;G)
Alt	rs770248150(A;A) rs770248150(G;G)
Reference	Rs770248150(T;T)
Significance	Pathogenic
Disease	Colorectal Neoplasms Oesophageal carcinoma Malignant melanoma of skin Multiple myeloma Hepatocellular carcinoma Adenocarcinoma of stomach
Variation	info
Gene	KRAS
CLNDBN	Colorectal Neoplasms Oesophageal carcinoma Malignant melanoma of skin Multiple myeloma Hepatocellular carcinoma Adenocarcinoma of stomach
Reversed	0
HGVS	NC_000012.11:g.25378647T>A; NC_000012.11:g.25378647T>G
CLNSRC
CLNACC	RCV000433195.1, RCV000425583.1, RCV000425803.1, RCV000435219.1, RCV000435839.1, RCV000442858.1, RCV000443670.1,