rs606231397

Merged into

rs276174811

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;T)	6	BRCA2 variant considered pathogenic for breast cancer

Make rs606231397(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32333086

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs606231397
dbSNP (classic)	rs606231397
ClinGen	rs606231397
ebi	rs606231397
HLI	rs606231397
Exac	rs606231397
Gnomad	rs606231397
Varsome	rs606231397
LitVar	rs606231397
Map	rs606231397
PheGenI	rs606231397
Biobank	rs606231397
1000 genomes	rs606231397
hgdp	rs606231397
ensembl	rs606231397
geneview	rs606231397
scholar	rs606231397
google	rs606231397
pharmgkb	rs606231397
gwascentral	rs606231397
openSNP	rs606231397
23andMe	rs606231397
SNPshot	rs606231397
SNPdbe	rs606231397
MSV3d	rs606231397
GWAS Ctlg	rs606231397

Status

Merged into rs276174811

Max Magnitude

6

rs606231397 has merged into rs276174811

ClinVar
Risk	rs606231397(T;T)
Alt	rs606231397(T;T)
Reference	Rs606231397(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32907223dupT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000112942.2,