rs397508048

Orientation

plus

Stabilized

plus

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

Make rs397508048(G;G)

Make rs397508048(G;TA)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394788

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508048
dbSNP (classic)	rs397508048
ClinGen	rs397508048
ebi	rs397508048
HLI	rs397508048
Exac	rs397508048
Gnomad	rs397508048
Varsome	rs397508048
LitVar	rs397508048
Map	rs397508048
PheGenI	rs397508048
Biobank	rs397508048
1000 genomes	rs397508048
hgdp	rs397508048
ensembl	rs397508048
geneview	rs397508048
scholar	rs397508048
google	rs397508048
pharmgkb	rs397508048
gwascentral	rs397508048
openSNP	rs397508048
23andMe	rs397508048
SNPshot	rs397508048
SNPdbe	rs397508048
MSV3d	rs397508048
GWAS Ctlg	rs397508048

Max Magnitude

0

ClinVar
Risk	rs397508048(G;G)
Alt	rs397508048(G;G)
Reference	Rs397508048(TA;TA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32968925_32968926delTAinsG
CLNSRC	ClinVar
CLNACC	RCV000045799.2,