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rs104894951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894951(A;A)
Make rs104894951(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38675778
GeneTSPAN7
is asnp
is mentioned by
dbSNPrs104894951
ebirs104894951
HLIrs104894951
Exacrs104894951
Varsomers104894951
Maprs104894951
PheGenIrs104894951
hapmaprs104894951
1000 genomesrs104894951
hgdprs104894951
ensemblrs104894951
gopubmedrs104894951
geneviewrs104894951
scholarrs104894951
googlers104894951
pharmgkbrs104894951
gwascentralrs104894951
openSNPrs104894951
23andMers104894951
23andMe allrs104894951
SNP Nexus

SNPshotrs104894951
SNPdbers104894951
MSV3drs104894951
GWAS Ctlgrs104894951
Max Magnitude0
OMIM300096
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894951(A,G;A,G)
Alt rs104894951(A,G;A,G)
Reference rs104894951(C;C)
Significance Pathogenic
Disease Mental retardation 58
Variation info
Gene TSPAN7
CLNDBN Mental retardation 58, X-linked
Reversed 0
HGVS NC_000023.10:g.38535032C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012396.22,