rs747887601

Orientation

plus

Stabilized

plus

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

Make rs747887601(C;C)

Make rs747887601(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

8234907

Gene

CTC1

is a	snp
is	mentioned by
dbSNP	rs747887601
dbSNP (classic)	rs747887601
ClinGen	rs747887601
ebi	rs747887601
HLI	rs747887601
Exac	rs747887601
Gnomad	rs747887601
Varsome	rs747887601
LitVar	rs747887601
Map	rs747887601
PheGenI	rs747887601
Biobank	rs747887601
1000 genomes	rs747887601
hgdp	rs747887601
ensembl	rs747887601
geneview	rs747887601
scholar	rs747887601
google	rs747887601
pharmgkb	rs747887601
gwascentral	rs747887601
openSNP	rs747887601
23andMe	rs747887601
SNPshot	rs747887601
SNPdbe	rs747887601
MSV3d	rs747887601
GWAS Ctlg	rs747887601

Max Magnitude

0

ClinVar
Risk	rs747887601(C;C)
Alt	rs747887601(C;C)
Reference	Rs747887601(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CTC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.8138225T>C
CLNSRC
CLNACC	RCV000428927.1,