rs397507274

Orientation

plus

Stabilized

plus

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

Make rs397507274(A;A)

Make rs397507274(A;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333183

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507274
dbSNP (classic)	rs397507274
ClinGen	rs397507274
ebi	rs397507274
HLI	rs397507274
Exac	rs397507274
Gnomad	rs397507274
Varsome	rs397507274
LitVar	rs397507274
Map	rs397507274
PheGenI	rs397507274
Biobank	rs397507274
1000 genomes	rs397507274
hgdp	rs397507274
ensembl	rs397507274
geneview	rs397507274
scholar	rs397507274
google	rs397507274
pharmgkb	rs397507274
gwascentral	rs397507274
openSNP	rs397507274
23andMe	rs397507274
SNPshot	rs397507274
SNPdbe	rs397507274
MSV3d	rs397507274
GWAS Ctlg	rs397507274

Max Magnitude

0

ClinVar
Risk	rs397507274(A;A)
Alt	rs397507274(A;A)
Reference	Rs397507274(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32907320C>A
CLNSRC	ClinVar
CLNACC	RCV000215568.1, RCV000220050.1, RCV000470503.1,