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rs122459146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs122459146(A;A)
Make rs122459146(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136207909
GeneFHL1
is asnp
is mentioned by
dbSNPrs122459146
ebirs122459146
HLIrs122459146
Exacrs122459146
Varsomers122459146
Maprs122459146
PheGenIrs122459146
hapmaprs122459146
1000 genomesrs122459146
hgdprs122459146
ensemblrs122459146
gopubmedrs122459146
geneviewrs122459146
scholarrs122459146
googlers122459146
pharmgkbrs122459146
gwascentralrs122459146
openSNPrs122459146
23andMers122459146
23andMe allrs122459146
SNP Nexus

SNPshotrs122459146
SNPdbers122459146
MSV3drs122459146
GWAS Ctlgrs122459146
Max Magnitude0
OMIM300163
Desc
Variant0008
Relatedalso
ClinVar
Risk rs122459146(A;A)
Alt rs122459146(A;A)
Reference rs122459146(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene FHL1
CLNDBN Myopathy, reducing body, X-linked, early-onset, severe
Reversed 0
HGVS NC_000023.10:g.135290068G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012310.23,