rs397508044

Orientation

plus

Stabilized

plus

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

Make rs397508044(A;A)

Make rs397508044(A;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394723

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508044
dbSNP (classic)	rs397508044
ClinGen	rs397508044
ebi	rs397508044
HLI	rs397508044
Exac	rs397508044
Gnomad	rs397508044
Varsome	rs397508044
LitVar	rs397508044
Map	rs397508044
PheGenI	rs397508044
Biobank	rs397508044
1000 genomes	rs397508044
hgdp	rs397508044
ensembl	rs397508044
geneview	rs397508044
scholar	rs397508044
google	rs397508044
pharmgkb	rs397508044
gwascentral	rs397508044
openSNP	rs397508044
23andMe	rs397508044
SNPshot	rs397508044
SNPdbe	rs397508044
MSV3d	rs397508044
GWAS Ctlg	rs397508044

Max Magnitude

0

ClinVar
Risk	rs397508044(A;A)
Alt	rs397508044(A;A)
Reference	Rs397508044(T;T)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32968860T>A
CLNSRC	ClinVar
CLNACC	RCV000045781.2,