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rs1800751

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs1800751(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047676
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1800751
ebirs1800751
HLIrs1800751
Exacrs1800751
Varsomers1800751
Maprs1800751
PheGenIrs1800751
hapmaprs1800751
1000 genomesrs1800751
hgdprs1800751
ensemblrs1800751
gopubmedrs1800751
geneviewrs1800751
scholarrs1800751
googlers1800751
pharmgkbrs1800751
gwascentralrs1800751
openSNPrs1800751
23andMers1800751
23andMe allrs1800751
SNP Nexus

SNPshotrs1800751
SNPdbers1800751
MSV3drs1800751
GWAS Ctlgrs1800751
Max Magnitude0
ClinVar
Risk rs1800751(G,T;G,T)
Alt rs1800751(G,T;G,T)
Reference rs1800751(C;C)
Significance Untested
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41199693G>C
CLNSRC ClinVar
CLNACC RCV000031251.5, RCV000048994.2,



[PMID 17719744] Identification and in silico analysis of functional SNPs of the BRCA1 gene.