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rs368817785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368817785(A;A)
Make rs368817785(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position77285548
GenePOMT2
is asnp
is mentioned by
dbSNPrs368817785
ebirs368817785
HLIrs368817785
Exacrs368817785
Varsomers368817785
Maprs368817785
PheGenIrs368817785
hapmaprs368817785
1000 genomesrs368817785
hgdprs368817785
ensemblrs368817785
gopubmedrs368817785
geneviewrs368817785
scholarrs368817785
googlers368817785
pharmgkbrs368817785
gwascentralrs368817785
openSNPrs368817785
23andMers368817785
23andMe allrs368817785
SNP Nexus

SNPshotrs368817785
SNPdbers368817785
MSV3drs368817785
GWAS Ctlgrs368817785
Max Magnitude0
ClinVar
Risk rs368817785(A;A)
Alt rs368817785(A;A)
Reference rs368817785(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POMT2
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.77751891G>A
CLNSRC ClinVar Emory University
CLNACC RCV000081565.5,