rs397509303

Orientation

minus

Stabilized

minus

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

Make rs397509303(-;T)

Make rs397509303(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43124034

Gene	BRCA1, NBR2

is a	snp
is	mentioned by
dbSNP	rs397509303
dbSNP (classic)	rs397509303
ClinGen	rs397509303
ebi	rs397509303
HLI	rs397509303
Exac	rs397509303
Gnomad	rs397509303
Varsome	rs397509303
LitVar	rs397509303
Map	rs397509303
PheGenI	rs397509303
Biobank	rs397509303
1000 genomes	rs397509303
hgdp	rs397509303
ensembl	rs397509303
geneview	rs397509303
scholar	rs397509303
google	rs397509303
pharmgkb	rs397509303
gwascentral	rs397509303
openSNP	rs397509303
23andMe	rs397509303
SNPshot	rs397509303
SNPdbe	rs397509303
MSV3d	rs397509303
GWAS Ctlg	rs397509303

Max Magnitude

0

ClinVar
Risk	rs397509303(T;T)
Alt	rs397509303(T;T)
Reference	Rs397509303(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	NBR2 BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41276052dupA
CLNSRC	ClinVar
CLNACC	RCV000049075.2,