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rs104893683

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893683(A;A)
Make rs104893683(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position161085944
GeneB3GALNT1
is asnp
is mentioned by
dbSNPrs104893683
ebirs104893683
HLIrs104893683
Exacrs104893683
Varsomers104893683
Maprs104893683
PheGenIrs104893683
hapmaprs104893683
1000 genomesrs104893683
hgdprs104893683
ensemblrs104893683
gopubmedrs104893683
geneviewrs104893683
scholarrs104893683
googlers104893683
pharmgkbrs104893683
gwascentralrs104893683
openSNPrs104893683
23andMers104893683
23andMe allrs104893683
SNP Nexus

SNPshotrs104893683
SNPdbers104893683
MSV3drs104893683
GWAS Ctlgrs104893683
Max Magnitude0
OMIM603094
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893683(A;A)
Alt rs104893683(A;A)
Reference rs104893683(G;G)
Significance Other
Disease p phenotype
Variation info
Gene B3GALNT1
CLNDBN p phenotype
Reversed 1
HGVS NC_000003.11:g.160803732C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007014.3,