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rs786202064

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202064(C;T)
Make rs786202064(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43071080
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202064
ebirs786202064
HLIrs786202064
Exacrs786202064
Varsomers786202064
Maprs786202064
PheGenIrs786202064
hapmaprs786202064
1000 genomesrs786202064
hgdprs786202064
ensemblrs786202064
gopubmedrs786202064
geneviewrs786202064
scholarrs786202064
googlers786202064
pharmgkbrs786202064
gwascentralrs786202064
openSNPrs786202064
23andMers786202064
23andMe allrs786202064
SNP Nexus

SNPshotrs786202064
SNPdbers786202064
MSV3drs786202064
GWAS Ctlgrs786202064
Max Magnitude0
ClinVar
Risk rs786202064(T;T)
Alt rs786202064(T;T)
Reference rs786202064(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41223097G>A
CLNSRC
CLNACC RCV000164690.1,