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rs775019409

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775019409(G;T)
Make rs775019409(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position15230953
GenePMP22
is asnp
is mentioned by
dbSNPrs775019409
ebirs775019409
HLIrs775019409
Exacrs775019409
Varsomers775019409
Maprs775019409
PheGenIrs775019409
hapmaprs775019409
1000 genomesrs775019409
hgdprs775019409
ensemblrs775019409
gopubmedrs775019409
geneviewrs775019409
scholarrs775019409
googlers775019409
pharmgkbrs775019409
gwascentralrs775019409
openSNPrs775019409
23andMers775019409
23andMe allrs775019409
SNP Nexus

SNPshotrs775019409
SNPdbers775019409
MSV3drs775019409
GWAS Ctlgrs775019409
Max Magnitude0
ClinVar
Risk rs775019409(A,T;A,T)
Alt rs775019409(A,T;A,T)
Reference rs775019409(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PMP22
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.15134270G>T
CLNSRC
CLNACC RCV000213954.1,