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rs761848742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761848742(C;T)
Make rs761848742(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position131521439
GenePOMT1
is asnp
is mentioned by
dbSNPrs761848742
dbSNP (classic)rs761848742
ClinGenrs761848742
ebirs761848742
HLIrs761848742
Exacrs761848742
Gnomadrs761848742
Varsomers761848742
LitVarrs761848742
Maprs761848742
PheGenIrs761848742
Biobankrs761848742
1000 genomesrs761848742
hgdprs761848742
ensemblrs761848742
geneviewrs761848742
scholarrs761848742
googlers761848742
pharmgkbrs761848742
gwascentralrs761848742
openSNPrs761848742
23andMers761848742
SNPshotrs761848742
SNPdbers761848742
MSV3drs761848742
GWAS Ctlgrs761848742
Max Magnitude0
ClinVar
Risk rs761848742(T;T)
Alt rs761848742(T;T)
Reference Rs761848742(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.134396826C>T
CLNSRC
CLNACC RCV000487062.1,