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rs786204675

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204675(-;-)
Make rs786204675(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position149978103
GeneSLC26A2
is asnp
is mentioned by
dbSNPrs786204675
ebirs786204675
HLIrs786204675
Exacrs786204675
Varsomers786204675
Maprs786204675
PheGenIrs786204675
hapmaprs786204675
1000 genomesrs786204675
hgdprs786204675
ensemblrs786204675
gopubmedrs786204675
geneviewrs786204675
scholarrs786204675
googlers786204675
pharmgkbrs786204675
gwascentralrs786204675
openSNPrs786204675
23andMers786204675
23andMe allrs786204675
SNP Nexus

SNPshotrs786204675
SNPdbers786204675
MSV3drs786204675
GWAS Ctlgrs786204675
Max Magnitude0
ClinVar
Risk rs786204675(;)
Alt rs786204675(;)
Reference rs786204675(T;T)
Significance Probable-Pathogenic
Disease Multiple epiphyseal dysplasia 4
Variation info
Gene SLC26A2
CLNDBN Multiple epiphyseal dysplasia 4
Reversed 0
HGVS NC_000005.9:g.149357666delT
CLNSRC
CLNACC RCV000169481.1,