rs397509319

Orientation

minus

Stabilized

minus

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

Make rs397509319(C;C)

Make rs397509319(C;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094743

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509319
dbSNP (classic)	rs397509319
ClinGen	rs397509319
ebi	rs397509319
HLI	rs397509319
Exac	rs397509319
Gnomad	rs397509319
Varsome	rs397509319
LitVar	rs397509319
Map	rs397509319
PheGenI	rs397509319
Biobank	rs397509319
1000 genomes	rs397509319
hgdp	rs397509319
ensembl	rs397509319
geneview	rs397509319
scholar	rs397509319
google	rs397509319
pharmgkb	rs397509319
gwascentral	rs397509319
openSNP	rs397509319
23andMe	rs397509319
SNPshot	rs397509319
SNPdbe	rs397509319
MSV3d	rs397509319
GWAS Ctlg	rs397509319

Max Magnitude

0

ClinVar
Risk	rs397509319(A;A) rs397509319(C;C) rs397509319(T;T)
Alt	rs397509319(A;A) rs397509319(C;C) rs397509319(T;T)
Reference	Rs397509319(G;G)
Significance	Untested
Disease	Familial cancer of breast not specified Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast not specified Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41246760C>A; NC_000017.10:g.41246760C>G; NC_000017.10:g.41246760C>T
CLNSRC	ClinVar
CLNACC	RCV000049133.2, RCV000049132.2, RCV000159945.1, RCV000165328.2, RCV000409328.1,