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rs267607063

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607063(C;T)
Make rs267607063(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position67052776
GeneSLC35D1
is asnp
is mentioned by
dbSNPrs267607063
ebirs267607063
HLIrs267607063
Exacrs267607063
Varsomers267607063
Maprs267607063
PheGenIrs267607063
hapmaprs267607063
1000 genomesrs267607063
hgdprs267607063
ensemblrs267607063
gopubmedrs267607063
geneviewrs267607063
scholarrs267607063
googlers267607063
pharmgkbrs267607063
gwascentralrs267607063
openSNPrs267607063
23andMers267607063
23andMe allrs267607063
SNP Nexus

SNPshotrs267607063
SNPdbers267607063
MSV3drs267607063
GWAS Ctlgrs267607063
Max Magnitude0
ClinVar
Risk rs267607063(G,T;G,T)
Alt rs267607063(G,T;G,T)
Reference rs267607063(C;C)
Significance Pathogenic
Disease Schneckenbecken dysplasia
Variation info
Gene SLC35D1
CLNDBN Schneckenbecken dysplasia
Reversed 1
HGVS NC_000001.10:g.67518459G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001185.2,