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rs724160005

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs724160005(A;G)
Make rs724160005(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position94576404
GeneTGDS
is asnp
is mentioned by
dbSNPrs724160005
ebirs724160005
HLIrs724160005
Exacrs724160005
Varsomers724160005
Maprs724160005
PheGenIrs724160005
hapmaprs724160005
1000 genomesrs724160005
hgdprs724160005
ensemblrs724160005
gopubmedrs724160005
geneviewrs724160005
scholarrs724160005
googlers724160005
pharmgkbrs724160005
gwascentralrs724160005
openSNPrs724160005
23andMers724160005
23andMe allrs724160005
SNP Nexus

SNPshotrs724160005
SNPdbers724160005
MSV3drs724160005
GWAS Ctlgrs724160005
Max Magnitude0
ClinVar
Risk rs724160005(G;G)
Alt rs724160005(G;G)
Reference rs724160005(A;A)
Significance Pathogenic
Disease Catel Manzke syndrome
Variation info
Gene TGDS
CLNDBN Catel Manzke syndrome
Reversed 1
HGVS NC_000013.10:g.95228658T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000149822.4,