rs606231401

Merged into

rs80359439

Orientation

plus

Stabilized

plus

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

Make rs606231401(-;T)

Make rs606231401(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32338638

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs606231401
dbSNP (classic)	rs606231401
ClinGen	rs606231401
ebi	rs606231401
HLI	rs606231401
Exac	rs606231401
Gnomad	rs606231401
Varsome	rs606231401
LitVar	rs606231401
Map	rs606231401
PheGenI	rs606231401
Biobank	rs606231401
1000 genomes	rs606231401
hgdp	rs606231401
ensembl	rs606231401
geneview	rs606231401
scholar	rs606231401
google	rs606231401
pharmgkb	rs606231401
gwascentral	rs606231401
openSNP	rs606231401
23andMe	rs606231401
SNPshot	rs606231401
SNPdbe	rs606231401
MSV3d	rs606231401
GWAS Ctlg	rs606231401

Status

Merged into rs80359439

Max Magnitude

0

ClinVar
Risk	rs606231401(T;T)
Alt	rs606231401(T;T)
Reference	Rs606231401(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32912776dupT
CLNSRC	Breast Cancer Information Core (BRCA2) Inc.
CLNACC	RCV000031473.10, RCV000044387.5, RCV000130074.4, RCV000160287.2,