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rs104894221

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894221(C;T)
Make rs104894221(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position22625795
GeneFANCF
is asnp
is mentioned by
dbSNPrs104894221
ebirs104894221
HLIrs104894221
Exacrs104894221
Varsomers104894221
Maprs104894221
PheGenIrs104894221
hapmaprs104894221
1000 genomesrs104894221
hgdprs104894221
ensemblrs104894221
gopubmedrs104894221
geneviewrs104894221
scholarrs104894221
googlers104894221
pharmgkbrs104894221
gwascentralrs104894221
openSNPrs104894221
23andMers104894221
23andMe allrs104894221
SNP Nexus

SNPshotrs104894221
SNPdbers104894221
MSV3drs104894221
GWAS Ctlgrs104894221
Max Magnitude0
OMIM603467
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894221(G,T;G,T)
Alt rs104894221(G,T;G,T)
Reference rs104894221(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCF
CLNDBN Fanconi anemia, complementation group F
Reversed 1
HGVS NC_000011.9:g.22647341G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006714.3,