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rs727502809

From SNPedia

Orientationminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs727502809(-;-)
Make rs727502809(-;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position94590895
GeneTGDS
is asnp
is mentioned by
dbSNPrs727502809
ebirs727502809
HLIrs727502809
Exacrs727502809
Varsomers727502809
Maprs727502809
PheGenIrs727502809
hapmaprs727502809
1000 genomesrs727502809
hgdprs727502809
ensemblrs727502809
gopubmedrs727502809
geneviewrs727502809
scholarrs727502809
googlers727502809
pharmgkbrs727502809
gwascentralrs727502809
openSNPrs727502809
23andMers727502809
23andMe allrs727502809
SNP Nexus

SNPshotrs727502809
SNPdbers727502809
MSV3drs727502809
GWAS Ctlgrs727502809
Max Magnitude0
ClinVar
Risk rs727502809(;)
Alt rs727502809(;)
Reference rs727502809(GA;GA)
Significance Pathogenic
Disease Catel Manzke syndrome
Variation info
Gene TGDS
CLNDBN Catel Manzke syndrome
Reversed 1
HGVS NC_000013.10:g.95243149_95243150delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000149821.4,