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rs104893649

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893649(G;T)
Make rs104893649(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position181678529
GeneNEUROD1
is asnp
is mentioned by
dbSNPrs104893649
ebirs104893649
HLIrs104893649
Exacrs104893649
Varsomers104893649
Maprs104893649
PheGenIrs104893649
hapmaprs104893649
1000 genomesrs104893649
hgdprs104893649
ensemblrs104893649
gopubmedrs104893649
geneviewrs104893649
scholarrs104893649
googlers104893649
pharmgkbrs104893649
gwascentralrs104893649
openSNPrs104893649
23andMers104893649
23andMe allrs104893649
SNP Nexus

SNPshotrs104893649
SNPdbers104893649
MSV3drs104893649
GWAS Ctlgrs104893649
Max Magnitude0
OMIM601724
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893649(T;T)
Alt rs104893649(T;T)
Reference rs104893649(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene NEUROD1
CLNDBN Diabetes mellitus type 2
Reversed 1
HGVS NC_000002.11:g.182543256C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008303.4,