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rs1057521922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521922(C;T)
Make rs1057521922(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position35106990
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs1057521922
dbSNP (old)rs1057521922
ClinGenrs1057521922
ebirs1057521922
HLIrs1057521922
Exacrs1057521922
Gnomadrs1057521922
Varsomers1057521922
LitVarrs1057521922
Maprs1057521922
PheGenIrs1057521922
Biobankrs1057521922
1000 genomesrs1057521922
hgdprs1057521922
ensemblrs1057521922
gopubmedrs1057521922
geneviewrs1057521922
scholarrs1057521922
googlers1057521922
pharmgkbrs1057521922
gwascentralrs1057521922
openSNPrs1057521922
23andMers1057521922
23andMe allrs1057521922
SNPshotrs1057521922
SNPdbers1057521922
MSV3drs1057521922
GWAS Ctlgrs1057521922
Max Magnitude0
ClinVar
Risk rs1057521922(T;T)
Alt rs1057521922(T;T)
Reference Rs1057521922(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.33434009G>A
CLNSRC
CLNACC RCV000434639.1,