rs80356959

Orientation

minus

Stabilized

minus

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

Make rs80356959(C;C)

Make rs80356959(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43045761

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80356959
dbSNP (classic)	rs80356959
ClinGen	rs80356959
ebi	rs80356959
HLI	rs80356959
Exac	rs80356959
Gnomad	rs80356959
Varsome	rs80356959
LitVar	rs80356959
Map	rs80356959
PheGenI	rs80356959
Biobank	rs80356959
1000 genomes	rs80356959
hgdp	rs80356959
ensembl	rs80356959
geneview	rs80356959
scholar	rs80356959
google	rs80356959
pharmgkb	rs80356959
gwascentral	rs80356959
openSNP	rs80356959
23andMe	rs80356959
SNPshot	rs80356959
SNPdbe	rs80356959
MSV3d	rs80356959
GWAS Ctlg	rs80356959

Max Magnitude

0

ClinVar
Risk	rs80356959(C;C) rs80356959(G;G)
Alt	rs80356959(C;C) rs80356959(G;G)
Reference	Rs80356959(T;T)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.41197778A>C; NC_000017.10:g.41197778A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000049027.2, RCV000112688.1, RCV000130013.3, RCV000031260.5, RCV000049026.2, RCV000129546.3, RCV000236322.2,