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rs121917787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917787(C;T)
Make rs121917787(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10043065
GeneFANCD2
is asnp
is mentioned by
dbSNPrs121917787
ebirs121917787
HLIrs121917787
Exacrs121917787
Varsomers121917787
Maprs121917787
PheGenIrs121917787
hapmaprs121917787
1000 genomesrs121917787
hgdprs121917787
ensemblrs121917787
gopubmedrs121917787
geneviewrs121917787
scholarrs121917787
googlers121917787
pharmgkbrs121917787
gwascentralrs121917787
openSNPrs121917787
23andMers121917787
23andMe allrs121917787
SNP Nexus

SNPshotrs121917787
SNPdbers121917787
MSV3drs121917787
GWAS Ctlgrs121917787
Max Magnitude0
OMIM227646
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121917787(T;T)
Alt rs121917787(T;T)
Reference rs121917787(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCD2
CLNDBN Fanconi anemia, complementation group D2
Reversed 0
HGVS NC_000003.11:g.10084749C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012820.2,