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rs864622739

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622739(A;A)
Make rs864622739(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89315390
GeneFANCI
is asnp
is mentioned by
dbSNPrs864622739
ebirs864622739
HLIrs864622739
Exacrs864622739
Varsomers864622739
Maprs864622739
PheGenIrs864622739
hapmaprs864622739
1000 genomesrs864622739
hgdprs864622739
ensemblrs864622739
gopubmedrs864622739
geneviewrs864622739
scholarrs864622739
googlers864622739
pharmgkbrs864622739
gwascentralrs864622739
openSNPrs864622739
23andMers864622739
23andMe allrs864622739
SNP Nexus

SNPshotrs864622739
SNPdbers864622739
MSV3drs864622739
GWAS Ctlgrs864622739
Max Magnitude0
ClinVar
Risk rs864622739(A;A)
Alt rs864622739(A;A)
Reference rs864622739(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCI
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000015.9:g.89858621G>A
CLNSRC
CLNACC RCV000206316.1,