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rs121913607

From SNPedia

Merged intors121913595
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913607(A;A)
Make rs121913607(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position161306785
GeneMPZ
is asnp
is mentioned by
dbSNPrs121913607
ebirs121913607
HLIrs121913607
Exacrs121913607
Varsomers121913607
Maprs121913607
PheGenIrs121913607
hapmaprs121913607
1000 genomesrs121913607
hgdprs121913607
ensemblrs121913607
gopubmedrs121913607
geneviewrs121913607
scholarrs121913607
googlers121913607
pharmgkbrs121913607
gwascentralrs121913607
openSNPrs121913607
23andMers121913607
23andMe allrs121913607
SNP Nexus

SNPshotrs121913607
SNPdbers121913607
MSV3drs121913607
GWAS Ctlgrs121913607
StatusMerged into rs121913595
Max Magnitude0
OMIM159440
Desc
Variant0031
Relatedalso
ClinVar
Risk rs121913607(A;A)
Alt rs121913607(A;A)
Reference rs121913607(C;C)
Significance Pathogenic
Disease
Variation info
Gene MPZ
CLNDBN
Reversed 1
HGVS NC_000001.10:g.161276575G>T
CLNSRC
CLNACC