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

rs587776958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776958(A;C)
Make rs587776958(C;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position139454331
GeneLOC101927451, RAB33B
is asnp
is mentioned by
dbSNPrs587776958
ebirs587776958
HLIrs587776958
Exacrs587776958
Varsomers587776958
Maprs587776958
PheGenIrs587776958
hapmaprs587776958
1000 genomesrs587776958
hgdprs587776958
ensemblrs587776958
gopubmedrs587776958
geneviewrs587776958
scholarrs587776958
googlers587776958
pharmgkbrs587776958
gwascentralrs587776958
openSNPrs587776958
23andMers587776958
23andMe allrs587776958
SNP Nexus

SNPshotrs587776958
SNPdbers587776958
MSV3drs587776958
GWAS Ctlgrs587776958
Max Magnitude0
ClinVar
Risk rs587776958(C;C)
Alt rs587776958(C;C)
Reference rs587776958(A;A)
Significance Pathogenic
Disease Smith McCort dysplasia 2
Variation info
Gene RAB33B LOC101927451
CLNDBN Smith McCort dysplasia 2
Reversed 0
HGVS NC_000004.11:g.140375485A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000043483.3,