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rs786205625

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205625(-;-)
Make rs786205625(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position77283847
GenePOMT2
is asnp
is mentioned by
dbSNPrs786205625
ebirs786205625
HLIrs786205625
Exacrs786205625
Varsomers786205625
Maprs786205625
PheGenIrs786205625
hapmaprs786205625
1000 genomesrs786205625
hgdprs786205625
ensemblrs786205625
gopubmedrs786205625
geneviewrs786205625
scholarrs786205625
googlers786205625
pharmgkbrs786205625
gwascentralrs786205625
openSNPrs786205625
23andMers786205625
23andMe allrs786205625
SNP Nexus

SNPshotrs786205625
SNPdbers786205625
MSV3drs786205625
GWAS Ctlgrs786205625
Max Magnitude0
ClinVar
Risk rs786205625(;)
Alt rs786205625(;)
Reference rs786205625(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POMT2
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.77750190delG
CLNSRC
CLNACC RCV000171478.1,