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rs121908850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908850(A;A)
Make rs121908850(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position34026832
GeneALG10
is asnp
is mentioned by
dbSNPrs121908850
ebirs121908850
HLIrs121908850
Exacrs121908850
Varsomers121908850
Maprs121908850
PheGenIrs121908850
hapmaprs121908850
1000 genomesrs121908850
hgdprs121908850
ensemblrs121908850
gopubmedrs121908850
geneviewrs121908850
scholarrs121908850
googlers121908850
pharmgkbrs121908850
gwascentralrs121908850
openSNPrs121908850
23andMers121908850
23andMe allrs121908850
SNP Nexus

SNPshotrs121908850
SNPdbers121908850
MSV3drs121908850
GWAS Ctlgrs121908850
Max Magnitude0
OMIM603313
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908850(A;A)
Alt rs121908850(A;A)
Reference rs121908850(G;G)
Significance Other
Disease Long QT syndrome 2
Variation info
Gene ALG10
CLNDBN Long QT syndrome 2
Reversed 0
HGVS NC_000012.11:g.34179767G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006869.2,