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rs267607000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607000(A;A)
Make rs267607000(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position47180493
GeneRBM10
is asnp
is mentioned by
dbSNPrs267607000
ebirs267607000
HLIrs267607000
Exacrs267607000
Varsomers267607000
Maprs267607000
PheGenIrs267607000
hapmaprs267607000
1000 genomesrs267607000
hgdprs267607000
ensemblrs267607000
gopubmedrs267607000
geneviewrs267607000
scholarrs267607000
googlers267607000
pharmgkbrs267607000
gwascentralrs267607000
openSNPrs267607000
23andMers267607000
23andMe allrs267607000
SNP Nexus

SNPshotrs267607000
SNPdbers267607000
MSV3drs267607000
GWAS Ctlgrs267607000
Max Magnitude0
ClinVar
Risk rs267607000(A;A)
Alt rs267607000(A;A)
Reference rs267607000(G;G)
Significance Pathogenic
Disease TARP syndrome
Variation info
Gene RBM10
CLNDBN TARP syndrome
Reversed 0
HGVS NC_000023.10:g.47039892G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012410.24,