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rs1064795775

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position43094254
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1064795775
dbSNP (old)rs1064795775
ClinGenrs1064795775
ebirs1064795775
HLIrs1064795775
Exacrs1064795775
Gnomadrs1064795775
Varsomers1064795775
Maprs1064795775
PheGenIrs1064795775
Biobankrs1064795775
1000 genomesrs1064795775
hgdprs1064795775
ensemblrs1064795775
gopubmedrs1064795775
geneviewrs1064795775
scholarrs1064795775
googlers1064795775
pharmgkbrs1064795775
gwascentralrs1064795775
openSNPrs1064795775
23andMers1064795775
23andMe allrs1064795775
SNPshotrs1064795775
SNPdbers1064795775
MSV3drs1064795775
GWAS Ctlgrs1064795775
Max Magnitude0
ClinVar
Risk rs1064795775(-;-)
Alt rs1064795775(-;-)
Reference Rs1064795775(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.41246271delG
CLNSRC
CLNACC RCV000480796.1,