rs606231398

Merged into

rs80359306

Orientation

plus

Stabilized

plus

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

Make rs606231398(-;A)

Make rs606231398(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32333285

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs606231398
ClinGen	rs606231398
ebi	rs606231398
HLI	rs606231398
Exac	rs606231398
Varsome	rs606231398
Map	rs606231398
PheGenI	rs606231398
hapmap	rs606231398
1000 genomes	rs606231398
hgdp	rs606231398
ensembl	rs606231398
gopubmed	rs606231398
geneview	rs606231398
scholar	rs606231398
google	rs606231398
pharmgkb	rs606231398
gwascentral	rs606231398
openSNP	rs606231398
23andMe	rs606231398
23andMe all	rs606231398
SNP Nexus
SNPshot	rs606231398
SNPdbe	rs606231398
MSV3d	rs606231398
GWAS Ctlg	rs606231398

Status

Merged into rs80359306

Max Magnitude

0

ClinVar
Risk	rs606231398(A;A)
Alt	rs606231398(A;A)
Reference	Rs606231398(;)
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.32907428dupA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031343.13, RCV000043897.6, RCV000131453.3, RCV000160269.2,