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rs759877008

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759877008(A;A)
Make rs759877008(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89805275
GeneFANCA
is asnp
is mentioned by
dbSNPrs759877008
ebirs759877008
HLIrs759877008
Exacrs759877008
Varsomers759877008
Maprs759877008
PheGenIrs759877008
hapmaprs759877008
1000 genomesrs759877008
hgdprs759877008
ensemblrs759877008
gopubmedrs759877008
geneviewrs759877008
scholarrs759877008
googlers759877008
pharmgkbrs759877008
gwascentralrs759877008
openSNPrs759877008
23andMers759877008
23andMe allrs759877008
SNP Nexus

SNPshotrs759877008
SNPdbers759877008
MSV3drs759877008
GWAS Ctlgrs759877008
Max Magnitude0
ClinVar
Risk rs759877008(A,T;A,T)
Alt rs759877008(A,T;A,T)
Reference rs759877008(C;C)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000016.9:g.89871683C>A
CLNSRC
CLNACC RCV000233245.1,