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rs797044941

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044941(C;C)
Make rs797044941(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161306776
GeneMPZ
is asnp
is mentioned by
dbSNPrs797044941
ebirs797044941
HLIrs797044941
Exacrs797044941
Varsomers797044941
Maprs797044941
PheGenIrs797044941
hapmaprs797044941
1000 genomesrs797044941
hgdprs797044941
ensemblrs797044941
gopubmedrs797044941
geneviewrs797044941
scholarrs797044941
googlers797044941
pharmgkbrs797044941
gwascentralrs797044941
openSNPrs797044941
23andMers797044941
23andMe allrs797044941
SNP Nexus

SNPshotrs797044941
SNPdbers797044941
MSV3drs797044941
GWAS Ctlgrs797044941
Max Magnitude0
ClinVar
Risk rs797044941(C;C)
Alt rs797044941(C;C)
Reference rs797044941(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene MPZ
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000001.10:g.161276566C>G
CLNSRC
CLNACC RCV000190787.1,