rs397507404

Orientation

plus

Stabilized

plus

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

Make rs397507404(A;A)

Make rs397507404(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32370955

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507404
dbSNP (classic)	rs397507404
ClinGen	rs397507404
ebi	rs397507404
HLI	rs397507404
Exac	rs397507404
Gnomad	rs397507404
Varsome	rs397507404
LitVar	rs397507404
Map	rs397507404
PheGenI	rs397507404
Biobank	rs397507404
1000 genomes	rs397507404
hgdp	rs397507404
ensembl	rs397507404
geneview	rs397507404
scholar	rs397507404
google	rs397507404
pharmgkb	rs397507404
gwascentral	rs397507404
openSNP	rs397507404
23andMe	rs397507404
SNPshot	rs397507404
SNPdbe	rs397507404
MSV3d	rs397507404
GWAS Ctlg	rs397507404

Max Magnitude

0

ClinVar
Risk	rs397507404(A;A) rs397507404(T;T)
Alt	rs397507404(A;A) rs397507404(T;T)
Reference	Rs397507404(G;G)
Significance	Other
Disease	Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32945092G>A; NC_000013.10:g.32945092G>T
CLNSRC	ClinVar
CLNACC	RCV000031747.3, RCV000160152.3, RCV000213906.1, RCV000231355.2, RCV000258314.1,