Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894222(C;G)
Make rs104894222(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position22625484
GeneFANCF
is asnp
is mentioned by
dbSNPrs104894222
ebirs104894222
HLIrs104894222
Exacrs104894222
Varsomers104894222
Maprs104894222
PheGenIrs104894222
hapmaprs104894222
1000 genomesrs104894222
hgdprs104894222
ensemblrs104894222
gopubmedrs104894222
geneviewrs104894222
scholarrs104894222
googlers104894222
pharmgkbrs104894222
gwascentralrs104894222
openSNPrs104894222
23andMers104894222
23andMe allrs104894222
SNP Nexus

SNPshotrs104894222
SNPdbers104894222
MSV3drs104894222
GWAS Ctlgrs104894222
Max Magnitude0
OMIM603467
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894222(G;G)
Alt rs104894222(G;G)
Reference rs104894222(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCF
CLNDBN Fanconi anemia, complementation group F
Reversed 1
HGVS NC_000011.9:g.22647030G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006716.2,