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

rs104894688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894688(C;T)
Make rs104894688(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position48750456
GeneFUT1
is asnp
is mentioned by
dbSNPrs104894688
ebirs104894688
HLIrs104894688
Exacrs104894688
Varsomers104894688
Maprs104894688
PheGenIrs104894688
hapmaprs104894688
1000 genomesrs104894688
hgdprs104894688
ensemblrs104894688
gopubmedrs104894688
geneviewrs104894688
scholarrs104894688
googlers104894688
pharmgkbrs104894688
gwascentralrs104894688
openSNPrs104894688
23andMers104894688
23andMe allrs104894688
SNP Nexus

SNPshotrs104894688
SNPdbers104894688
MSV3drs104894688
GWAS Ctlgrs104894688
Max Magnitude0
OMIM211100
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894688(T;T)
Alt rs104894688(T;T)
Reference rs104894688(C;C)
Significance Pathogenic
Disease Para-Bombay phenotype
Variation info
Gene FUT1
CLNDBN Para-Bombay phenotype
Reversed 1
HGVS NC_000019.9:g.49253713G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012924.17,