rs1057517636

Orientation

plus

Stabilized

plus

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

Make rs1057517636(A;T)

Make rs1057517636(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32338829

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1057517636
dbSNP (classic)	rs1057517636
ClinGen	rs1057517636
ebi	rs1057517636
HLI	rs1057517636
Exac	rs1057517636
Gnomad	rs1057517636
Varsome	rs1057517636
LitVar	rs1057517636
Map	rs1057517636
PheGenI	rs1057517636
Biobank	rs1057517636
1000 genomes	rs1057517636
hgdp	rs1057517636
ensembl	rs1057517636
geneview	rs1057517636
scholar	rs1057517636
google	rs1057517636
pharmgkb	rs1057517636
gwascentral	rs1057517636
openSNP	rs1057517636
23andMe	rs1057517636
SNPshot	rs1057517636
SNPdbe	rs1057517636
MSV3d	rs1057517636
GWAS Ctlg	rs1057517636

Max Magnitude

0

ClinVar
Risk	rs1057517636(T;T)
Alt	rs1057517636(T;T)
Reference	Rs1057517636(A;A)
Significance	Probable-Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912966A>T
CLNSRC
CLNACC	RCV000411097.1,