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rs1060502601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502601(-;-)
Make rs1060502601(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position58709885
GeneRAD51C
is asnp
is mentioned by
dbSNPrs1060502601
dbSNP (old)rs1060502601
ClinGenrs1060502601
ebirs1060502601
HLIrs1060502601
Exacrs1060502601
Gnomadrs1060502601
Varsomers1060502601
Maprs1060502601
PheGenIrs1060502601
Biobankrs1060502601
1000 genomesrs1060502601
hgdprs1060502601
ensemblrs1060502601
gopubmedrs1060502601
geneviewrs1060502601
scholarrs1060502601
googlers1060502601
pharmgkbrs1060502601
gwascentralrs1060502601
openSNPrs1060502601
23andMers1060502601
23andMe allrs1060502601
SNPshotrs1060502601
SNPdbers1060502601
MSV3drs1060502601
GWAS Ctlgrs1060502601
Max Magnitude0
ClinVar
Risk rs1060502601(-;-)
Alt rs1060502601(-;-)
Reference Rs1060502601(T;T)
Significance Pathogenic
Disease Fanconi anemia not provided
Variation info
Gene RAD51C
CLNDBN Fanconi anemia, complementation group O not provided
Reversed 0
HGVS NC_000017.10:g.56787246delT
CLNSRC
CLNACC RCV000471345.1, RCV000486595.1,