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rs1057518021

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518021(C;C)
Make rs1057518021(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position161307425
GeneMPZ
is asnp
is mentioned by
dbSNPrs1057518021
dbSNP (old)rs1057518021
ClinGenrs1057518021
ebirs1057518021
HLIrs1057518021
Exacrs1057518021
Gnomadrs1057518021
Varsomers1057518021
Maprs1057518021
PheGenIrs1057518021
Biobankrs1057518021
1000 genomesrs1057518021
hgdprs1057518021
ensemblrs1057518021
gopubmedrs1057518021
geneviewrs1057518021
scholarrs1057518021
googlers1057518021
pharmgkbrs1057518021
gwascentralrs1057518021
openSNPrs1057518021
23andMers1057518021
23andMe allrs1057518021
SNPshotrs1057518021
SNPdbers1057518021
MSV3drs1057518021
GWAS Ctlgrs1057518021
Max Magnitude0
ClinVar
Risk rs1057518021(C;C)
Alt rs1057518021(C;C)
Reference Rs1057518021(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MPZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161277215C>G
CLNSRC
CLNACC RCV000412954.1,