rs397508035

Orientation

plus

Stabilized

plus

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

Make rs397508035(-;-)

Make rs397508035(-;AAAA)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379890

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508035
dbSNP (classic)	rs397508035
ClinGen	rs397508035
ebi	rs397508035
HLI	rs397508035
Exac	rs397508035
Gnomad	rs397508035
Varsome	rs397508035
LitVar	rs397508035
Map	rs397508035
PheGenI	rs397508035
Biobank	rs397508035
1000 genomes	rs397508035
hgdp	rs397508035
ensembl	rs397508035
geneview	rs397508035
scholar	rs397508035
google	rs397508035
pharmgkb	rs397508035
gwascentral	rs397508035
openSNP	rs397508035
23andMe	rs397508035
SNPshot	rs397508035
SNPdbe	rs397508035
MSV3d	rs397508035
GWAS Ctlg	rs397508035

Max Magnitude

0

ClinVar
Risk	rs397508035(-;-)
Alt	rs397508035(-;-)
Reference	Rs397508035(AAAA;AAAA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32954027_32954030delAAAA
CLNSRC	ClinVar
CLNACC	RCV000045709.2,