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rs121917784

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917784(C;T)
Make rs121917784(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position95249255
GeneFANCC
is asnp
is mentioned by
dbSNPrs121917784
ebirs121917784
HLIrs121917784
Exacrs121917784
Varsomers121917784
Maprs121917784
PheGenIrs121917784
hapmaprs121917784
1000 genomesrs121917784
hgdprs121917784
ensemblrs121917784
gopubmedrs121917784
geneviewrs121917784
scholarrs121917784
googlers121917784
pharmgkbrs121917784
gwascentralrs121917784
openSNPrs121917784
23andMers121917784
23andMe allrs121917784
SNP Nexus

SNPshotrs121917784
SNPdbers121917784
MSV3drs121917784
GWAS Ctlgrs121917784
Max Magnitude0
OMIM227645
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121917784(T;T)
Alt rs121917784(T;T)
Reference rs121917784(C;C)
Significance Other
Disease Fanconi anemia not provided
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C not provided
Reversed 1
HGVS NC_000009.11:g.98011537G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012826.6, RCV000115351.3,