rs397507768

Orientation

plus

Stabilized

plus

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

Make rs397507768(G;T)

Make rs397507768(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326499

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507768
dbSNP (classic)	rs397507768
ClinGen	rs397507768
ebi	rs397507768
HLI	rs397507768
Exac	rs397507768
Gnomad	rs397507768
Varsome	rs397507768
LitVar	rs397507768
Map	rs397507768
PheGenI	rs397507768
Biobank	rs397507768
1000 genomes	rs397507768
hgdp	rs397507768
ensembl	rs397507768
geneview	rs397507768
scholar	rs397507768
google	rs397507768
pharmgkb	rs397507768
gwascentral	rs397507768
openSNP	rs397507768
23andMe	rs397507768
SNPshot	rs397507768
SNPdbe	rs397507768
MSV3d	rs397507768
GWAS Ctlg	rs397507768

Max Magnitude

0

ClinVar
Risk	rs397507768(C;C) rs397507768(T;T)
Alt	rs397507768(C;C) rs397507768(T;T)
Reference	Rs397507768(G;G)
Significance	Pathogenic
Disease	not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32900636G>C; NC_000013.10:g.32900636G>T
CLNSRC	ClinVar
CLNACC	RCV000168537.4, RCV000222599.1, RCV000257907.2, RCV000258488.1, RCV000044593.2, RCV000220016.1, RCV000239003.1,