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rs121908435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908435(A;A)
Make rs121908435(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position115418391
GeneTRPS1
is asnp
is mentioned by
dbSNPrs121908435
ebirs121908435
HLIrs121908435
Exacrs121908435
Varsomers121908435
Maprs121908435
PheGenIrs121908435
hapmaprs121908435
1000 genomesrs121908435
hgdprs121908435
ensemblrs121908435
gopubmedrs121908435
geneviewrs121908435
scholarrs121908435
googlers121908435
pharmgkbrs121908435
gwascentralrs121908435
openSNPrs121908435
23andMers121908435
23andMe allrs121908435
SNP Nexus

SNPshotrs121908435
SNPdbers121908435
MSV3drs121908435
GWAS Ctlgrs121908435
Max Magnitude0
OMIM604386
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908435(A;A)
Alt rs121908435(A;A)
Reference rs121908435(G;G)
Significance Pathogenic
Disease Trichorhinophalangeal syndrome type 3
Variation info
Gene TRPS1
CLNDBN Trichorhinophalangeal syndrome type 3
Reversed 1
HGVS NC_000008.10:g.116430619C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005919.2,