rs121908707

Orientation

minus

Stabilized

minus

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

Make rs121908707(C;C)

Make rs121908707(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

28695709

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs121908707
dbSNP (classic)	rs121908707
ClinGen	rs121908707
ebi	rs121908707
HLI	rs121908707
Exac	rs121908707
Gnomad	rs121908707
Varsome	rs121908707
LitVar	rs121908707
Map	rs121908707
PheGenI	rs121908707
Biobank	rs121908707
1000 genomes	rs121908707
hgdp	rs121908707
ensembl	rs121908707
geneview	rs121908707
scholar	rs121908707
google	rs121908707
pharmgkb	rs121908707
gwascentral	rs121908707
openSNP	rs121908707
23andMe	rs121908707
SNPshot	rs121908707
SNPdbe	rs121908707
MSV3d	rs121908707
GWAS Ctlg	rs121908707

Max Magnitude

0

ClinVar
Risk	rs121908707(C;C) rs121908707(T;T)
Alt	rs121908707(C;C) rs121908707(T;T)
Reference	Rs121908707(G;G)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast not provided
Variation	info
Gene	CHEK2
CLNDBN	Familial cancer of breast not provided
Reversed	1
HGVS	NC_000022.10:g.29091697C>A; NC_000022.10:g.29091697C>G
CLNSRC
CLNACC	RCV000465281.1, RCV000114767.2,