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rs141952252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs141952252(A;G)
Make rs141952252(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position100017814
GeneSLC35A3
is asnp
is mentioned by
dbSNPrs141952252
ebirs141952252
HLIrs141952252
Exacrs141952252
Varsomers141952252
Maprs141952252
PheGenIrs141952252
hapmaprs141952252
1000 genomesrs141952252
hgdprs141952252
ensemblrs141952252
gopubmedrs141952252
geneviewrs141952252
scholarrs141952252
googlers141952252
pharmgkbrs141952252
gwascentralrs141952252
openSNPrs141952252
23andMers141952252
23andMe allrs141952252
SNP Nexus

SNPshotrs141952252
SNPdbers141952252
MSV3drs141952252
GWAS Ctlgrs141952252
Max Magnitude0
ClinVar
Risk rs141952252(G;G)
Alt rs141952252(G;G)
Reference rs141952252(A;A)
Significance Pathogenic
Disease Arthrogryposis
Variation info
Gene SLC35A3
CLNDBN Arthrogryposis, mental retardation, and seizures
Reversed 0
HGVS NC_000001.10:g.100483370A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000074504.4,