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rs1057517812

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1057517812(-;-)
Make rs1057517812(-;CA)
Make rs1057517812(CA;CA)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position58696849
GeneRAD51C
is asnp
is mentioned by
dbSNPrs1057517812
dbSNP (old)rs1057517812
ClinGenrs1057517812
ebirs1057517812
HLIrs1057517812
Exacrs1057517812
Gnomadrs1057517812
Varsomers1057517812
Maprs1057517812
PheGenIrs1057517812
Biobankrs1057517812
1000 genomesrs1057517812
hgdprs1057517812
ensemblrs1057517812
gopubmedrs1057517812
geneviewrs1057517812
scholarrs1057517812
googlers1057517812
pharmgkbrs1057517812
gwascentralrs1057517812
openSNPrs1057517812
23andMers1057517812
23andMe allrs1057517812
SNPshotrs1057517812
SNPdbers1057517812
MSV3drs1057517812
GWAS Ctlgrs1057517812
Max Magnitude0
ClinVar
Risk rs1057517812(-;-)
Alt rs1057517812(-;-)
Reference Rs1057517812(AC;AC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAD51C
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.56774210_56774211delCA
CLNSRC
CLNACC RCV000413272.1,