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rs724160004

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs724160004(A;G)
Make rs724160004(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position94590897
GeneTGDS
is asnp
is mentioned by
dbSNPrs724160004
ebirs724160004
HLIrs724160004
Exacrs724160004
Varsomers724160004
Maprs724160004
PheGenIrs724160004
hapmaprs724160004
1000 genomesrs724160004
hgdprs724160004
ensemblrs724160004
gopubmedrs724160004
geneviewrs724160004
scholarrs724160004
googlers724160004
pharmgkbrs724160004
gwascentralrs724160004
openSNPrs724160004
23andMers724160004
23andMe allrs724160004
SNP Nexus

SNPshotrs724160004
SNPdbers724160004
MSV3drs724160004
GWAS Ctlgrs724160004
Max Magnitude0
ClinVar
Risk rs724160004(G;G)
Alt rs724160004(G;G)
Reference rs724160004(A;A)
Significance Pathogenic
Disease Catel Manzke syndrome
Variation info
Gene TGDS
CLNDBN Catel Manzke syndrome
Reversed 1
HGVS NC_000013.10:g.95243151T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000149819.3,