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rs137853111

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853111(A;A)
Make rs137853111(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position67009112
GeneSLC35D1
is asnp
is mentioned by
dbSNPrs137853111
ebirs137853111
HLIrs137853111
Exacrs137853111
Varsomers137853111
Maprs137853111
PheGenIrs137853111
hapmaprs137853111
1000 genomesrs137853111
hgdprs137853111
ensemblrs137853111
gopubmedrs137853111
geneviewrs137853111
scholarrs137853111
googlers137853111
pharmgkbrs137853111
gwascentralrs137853111
openSNPrs137853111
23andMers137853111
23andMe allrs137853111
SNP Nexus

SNPshotrs137853111
SNPdbers137853111
MSV3drs137853111
GWAS Ctlgrs137853111
Max Magnitude0
OMIM610804
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853111(A;A)
Alt rs137853111(A;A)
Reference rs137853111(G;G)
Significance Pathogenic
Disease Schneckenbecken dysplasia
Variation info
Gene SLC35D1
CLNDBN Schneckenbecken dysplasia
Reversed 1
HGVS NC_000001.10:g.67474795C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001183.3,