rs397509316

Orientation

minus

Stabilized

minus

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

Make rs397509316(-;-)

Make rs397509316(-;A)

Make rs397509316(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094762

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509316
dbSNP (classic)	rs397509316
ClinGen	rs397509316
ebi	rs397509316
HLI	rs397509316
Exac	rs397509316
Gnomad	rs397509316
Varsome	rs397509316
LitVar	rs397509316
Map	rs397509316
PheGenI	rs397509316
Biobank	rs397509316
1000 genomes	rs397509316
hgdp	rs397509316
ensembl	rs397509316
geneview	rs397509316
scholar	rs397509316
google	rs397509316
pharmgkb	rs397509316
gwascentral	rs397509316
openSNP	rs397509316
23andMe	rs397509316
SNPshot	rs397509316
SNPdbe	rs397509316
MSV3d	rs397509316
GWAS Ctlg	rs397509316

Max Magnitude

0

ClinVar
Risk	rs397509316(A;A) rs397509316(AG;AG)
Alt	rs397509316(A;A) rs397509316(AG;AG)
Reference	rs397509316(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246779_41246780insCT; NC_000017.10:g.41246779_41246780insT
CLNSRC	ClinVar
CLNACC	RCV000049126.2, RCV000049125.2,