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rs267606813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606813(C;G)
Make rs267606813(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136207829
GeneFHL1
is asnp
is mentioned by
dbSNPrs267606813
ebirs267606813
HLIrs267606813
Exacrs267606813
Varsomers267606813
Maprs267606813
PheGenIrs267606813
hapmaprs267606813
1000 genomesrs267606813
hgdprs267606813
ensemblrs267606813
gopubmedrs267606813
geneviewrs267606813
scholarrs267606813
googlers267606813
pharmgkbrs267606813
gwascentralrs267606813
openSNPrs267606813
23andMers267606813
23andMe allrs267606813
SNP Nexus

SNPshotrs267606813
SNPdbers267606813
MSV3drs267606813
GWAS Ctlgrs267606813
Max Magnitude0
ClinVar
Risk rs267606813(G;G)
Alt rs267606813(G;G)
Reference rs267606813(C;C)
Significance Pathogenic
Disease Myopathy
Variation info
Gene FHL1
CLNDBN Myopathy, reducing body, X-linked, early-onset, severe
Reversed 0
HGVS NC_000023.10:g.135289988C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012318.25,