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rs876661257

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661257(G;T)
Make rs876661257(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position161306732
GeneMPZ
is asnp
is mentioned by
dbSNPrs876661257
ebirs876661257
HLIrs876661257
Exacrs876661257
Varsomers876661257
Maprs876661257
PheGenIrs876661257
hapmaprs876661257
1000 genomesrs876661257
hgdprs876661257
ensemblrs876661257
gopubmedrs876661257
geneviewrs876661257
scholarrs876661257
googlers876661257
pharmgkbrs876661257
gwascentralrs876661257
openSNPrs876661257
23andMers876661257
23andMe allrs876661257
SNP Nexus

SNPshotrs876661257
SNPdbers876661257
MSV3drs876661257
GWAS Ctlgrs876661257
Max Magnitude0
ClinVar
Risk rs876661257(T;T)
Alt rs876661257(T;T)
Reference rs876661257(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MPZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161276522C>A
CLNSRC
CLNACC RCV000216501.1,