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rs104894686

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894686(C;G)
Make rs104894686(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position48750334
GeneFUT1
is asnp
is mentioned by
dbSNPrs104894686
ebirs104894686
HLIrs104894686
Exacrs104894686
Varsomers104894686
Maprs104894686
PheGenIrs104894686
hapmaprs104894686
1000 genomesrs104894686
hgdprs104894686
ensemblrs104894686
gopubmedrs104894686
geneviewrs104894686
scholarrs104894686
googlers104894686
pharmgkbrs104894686
gwascentralrs104894686
openSNPrs104894686
23andMers104894686
23andMe allrs104894686
SNP Nexus

SNPshotrs104894686
SNPdbers104894686
MSV3drs104894686
GWAS Ctlgrs104894686
Max Magnitude0
OMIM211100
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894686(G,T;G,T)
Alt rs104894686(G,T;G,T)
Reference rs104894686(C;C)
Significance Other
Disease Bombay phenotype
Variation info
Gene FUT1
CLNDBN Bombay phenotype
Reversed 1
HGVS NC_000019.9:g.49253591G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012922.25,