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rs878854181

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854181(A;A)
Make rs878854181(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position89263422
GeneFANCI
is asnp
is mentioned by
dbSNPrs878854181
ebirs878854181
HLIrs878854181
Exacrs878854181
Varsomers878854181
Maprs878854181
PheGenIrs878854181
hapmaprs878854181
1000 genomesrs878854181
hgdprs878854181
ensemblrs878854181
gopubmedrs878854181
geneviewrs878854181
scholarrs878854181
googlers878854181
pharmgkbrs878854181
gwascentralrs878854181
openSNPrs878854181
23andMers878854181
23andMe allrs878854181
SNP Nexus

SNPshotrs878854181
SNPdbers878854181
MSV3drs878854181
GWAS Ctlgrs878854181
Max Magnitude0
ClinVar
Risk rs878854181(A;A)
Alt rs878854181(A;A)
Reference rs878854181(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCI
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000015.9:g.89806653G>A
CLNSRC
CLNACC RCV000230835.1,