rs8176318

minus

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

Make rs8176318(G;T)

Make rs8176318(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43045257

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs8176318
dbSNP (classic)	rs8176318
ClinGen	rs8176318
ebi	rs8176318
HLI	rs8176318
Exac	rs8176318
Gnomad	rs8176318
Varsome	rs8176318
LitVar	rs8176318
Map	rs8176318
PheGenI	rs8176318
Biobank	rs8176318
1000 genomes	rs8176318
hgdp	rs8176318
ensembl	rs8176318
geneview	rs8176318
scholar	rs8176318
google	rs8176318
pharmgkb	rs8176318
gwascentral	rs8176318
openSNP	rs8176318
23andMe	rs8176318
SNPshot	rs8176318
SNPdbe	rs8176318
MSV3d	rs8176318
GWAS Ctlg	rs8176318

GMAF

0.2906

Max Magnitude

0

?

(G;G) (G;T) (T;T)

28

[PMID 21191178 ] Rare BRCA1 haplotypes including 3'UTR SNPs associated with breast cancer risk

[PMID 17332845 ] Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.

[PMID 21161372 ] Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: potential modifying effect of BRCA1/BRCA2 mutation carrier status.

[PMID 24915755 ] A germline mutation in the BRCA1 3'UTR predicts Stage IV breast cancer

[PMID 26630397 ] SNP Regulation of microRNA Expression and Subsequent Colon Cancer Risk.

ClinVar
Risk	rs8176318(T;T)
Alt	rs8176318(T;T)
Reference	Rs8176318(G;G)
Significance	Probable-non-pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.41197274C>A
CLNSRC
CLNACC	RCV000191177.1, RCV000372376.1,