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rs1057517131

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517131(-;TC)
Make rs1057517131(TC;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95249182
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057517131
dbSNP (old)rs1057517131
ClinGenrs1057517131
ebirs1057517131
HLIrs1057517131
Exacrs1057517131
Gnomadrs1057517131
Varsomers1057517131
Maprs1057517131
PheGenIrs1057517131
Biobankrs1057517131
1000 genomesrs1057517131
hgdprs1057517131
ensemblrs1057517131
gopubmedrs1057517131
geneviewrs1057517131
scholarrs1057517131
googlers1057517131
pharmgkbrs1057517131
gwascentralrs1057517131
openSNPrs1057517131
23andMers1057517131
23andMe allrs1057517131
SNPshotrs1057517131
SNPdbers1057517131
MSV3drs1057517131
GWAS Ctlgrs1057517131
Max Magnitude0
ClinVar
Risk rs1057517131(TC;TC)
Alt rs1057517131(TC;TC)
Reference Rs1057517131(-;-)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.98011465_98011466dupGA
CLNSRC
CLNACC RCV000409107.1,