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rs3745635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3745635(A;A)
Make rs3745635(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position5844332
GeneFUT3
is asnp
is mentioned by
dbSNPrs3745635
ebirs3745635
HLIrs3745635
Exacrs3745635
Varsomers3745635
Maprs3745635
PheGenIrs3745635
hapmaprs3745635
1000 genomesrs3745635
hgdprs3745635
ensemblrs3745635
gopubmedrs3745635
geneviewrs3745635
scholarrs3745635
googlers3745635
pharmgkbrs3745635
gwascentralrs3745635
openSNPrs3745635
23andMers3745635
23andMe allrs3745635
SNP Nexus

SNPshotrs3745635
SNPdbers3745635
MSV3drs3745635
GWAS Ctlgrs3745635
GMAF0.1382
Max Magnitude0
OMIM111100
Desc
Variant0001
Relatedalso
ClinVar
Risk rs3745635(A;A)
Alt rs3745635(A;A)
Reference rs3745635(G;G)
Significance Other
Disease Le(-) PHENOTYPE
Variation info
Gene FUT3
CLNDBN Le(-) PHENOTYPE
Reversed 1
HGVS NC_000019.9:g.5844343C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019289.23,