Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909192(C;C)
Make rs121909192(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position70076545
GeneSMN2
is asnp
is mentioned by
dbSNPrs121909192
ebirs121909192
HLIrs121909192
Exacrs121909192
Varsomers121909192
Maprs121909192
PheGenIrs121909192
hapmaprs121909192
1000 genomesrs121909192
hgdprs121909192
ensemblrs121909192
gopubmedrs121909192
geneviewrs121909192
scholarrs121909192
googlers121909192
pharmgkbrs121909192
gwascentralrs121909192
openSNPrs121909192
23andMers121909192
23andMe allrs121909192
SNP Nexus

SNPshotrs121909192
SNPdbers121909192
MSV3drs121909192
GWAS Ctlgrs121909192
Max Magnitude0
OMIM601627
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909192(C;C)
Alt rs121909192(C;C)
Reference rs121909192(G;G)
Significance Other
Disease Spinal muscular atrophy
Variation info
Gene SMN2
CLNDBN Spinal muscular atrophy, modifier of
Reversed 0
HGVS NC_000005.9:g.69372372G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008426.3,