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rs1064794619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position35119612
GeneFNDC8, RAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs1064794619
dbSNP (classic)rs1064794619
ClinGenrs1064794619
ebirs1064794619
HLIrs1064794619
Exacrs1064794619
Gnomadrs1064794619
Varsomers1064794619
LitVarrs1064794619
Maprs1064794619
PheGenIrs1064794619
Biobankrs1064794619
1000 genomesrs1064794619
hgdprs1064794619
ensemblrs1064794619
geneviewrs1064794619
scholarrs1064794619
googlers1064794619
pharmgkbrs1064794619
gwascentralrs1064794619
openSNPrs1064794619
23andMers1064794619
23andMe allrs1064794619
SNPshotrs1064794619
SNPdbers1064794619
MSV3drs1064794619
GWAS Ctlgrs1064794619
Max Magnitude0
ClinVar
Risk rs1064794619(G;G)
Alt rs1064794619(G;G)
Reference Rs1064794619(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAD51D RAD51L3-RFFL FNDC8
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.33446631A>C
CLNSRC
CLNACC RCV000481968.1,