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rs1060502605

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CAAT;CAAT) 0 common in clinvar
Make rs1060502605(-;-)
Make rs1060502605(-;ATCA)
Make rs1060502605(ATCA;ATCA)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position58720759
GeneRAD51C
is asnp
is mentioned by
dbSNPrs1060502605
dbSNP (old)rs1060502605
ClinGenrs1060502605
ebirs1060502605
HLIrs1060502605
Exacrs1060502605
Gnomadrs1060502605
Varsomers1060502605
Maprs1060502605
PheGenIrs1060502605
Biobankrs1060502605
1000 genomesrs1060502605
hgdprs1060502605
ensemblrs1060502605
gopubmedrs1060502605
geneviewrs1060502605
scholarrs1060502605
googlers1060502605
pharmgkbrs1060502605
gwascentralrs1060502605
openSNPrs1060502605
23andMers1060502605
23andMe allrs1060502605
SNPshotrs1060502605
SNPdbers1060502605
MSV3drs1060502605
GWAS Ctlgrs1060502605
Max Magnitude0
ClinVar
Risk rs1060502605(-;-)
Alt rs1060502605(-;-)
Reference Rs1060502605(CAAT;CAAT)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene RAD51C
CLNDBN Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56798120_56798123delATCA
CLNSRC
CLNACC RCV000465331.1,