Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908430

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908430(A;A)
Make rs121908430(A;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position115604916
GeneTRPS1
is asnp
is mentioned by
dbSNPrs121908430
ebirs121908430
HLIrs121908430
Exacrs121908430
Varsomers121908430
Maprs121908430
PheGenIrs121908430
hapmaprs121908430
1000 genomesrs121908430
hgdprs121908430
ensemblrs121908430
gopubmedrs121908430
geneviewrs121908430
scholarrs121908430
googlers121908430
pharmgkbrs121908430
gwascentralrs121908430
openSNPrs121908430
23andMers121908430
23andMe allrs121908430
SNP Nexus

SNPshotrs121908430
SNPdbers121908430
MSV3drs121908430
GWAS Ctlgrs121908430
Max Magnitude0
OMIM604386
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908430(A;A)
Alt rs121908430(A;A)
Reference rs121908430(C;C)
Significance Pathogenic
Disease Trichorhinophalangeal dysplasia type I
Variation info
Gene TRPS1
CLNDBN Trichorhinophalangeal dysplasia type I
Reversed 1
HGVS NC_000008.10:g.116617143G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005911.2,