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rs876661287

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661287(G;T)
Make rs876661287(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position161307343
GeneMPZ
is asnp
is mentioned by
dbSNPrs876661287
ebirs876661287
HLIrs876661287
Exacrs876661287
Varsomers876661287
Maprs876661287
PheGenIrs876661287
hapmaprs876661287
1000 genomesrs876661287
hgdprs876661287
ensemblrs876661287
gopubmedrs876661287
geneviewrs876661287
scholarrs876661287
googlers876661287
pharmgkbrs876661287
gwascentralrs876661287
openSNPrs876661287
23andMers876661287
23andMe allrs876661287
SNP Nexus

SNPshotrs876661287
SNPdbers876661287
MSV3drs876661287
GWAS Ctlgrs876661287
Max Magnitude0
ClinVar
Risk rs876661287(T;T)
Alt rs876661287(T;T)
Reference rs876661287(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MPZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161277133C>A
CLNSRC
CLNACC RCV000223173.1,