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rs786200881

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786200881(-;-)
Make rs786200881(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position149978043
GeneSLC26A2
is asnp
is mentioned by
dbSNPrs786200881
ebirs786200881
HLIrs786200881
Exacrs786200881
Varsomers786200881
Maprs786200881
PheGenIrs786200881
hapmaprs786200881
1000 genomesrs786200881
hgdprs786200881
ensemblrs786200881
gopubmedrs786200881
geneviewrs786200881
scholarrs786200881
googlers786200881
pharmgkbrs786200881
gwascentralrs786200881
openSNPrs786200881
23andMers786200881
23andMe allrs786200881
SNP Nexus

SNPshotrs786200881
SNPdbers786200881
MSV3drs786200881
GWAS Ctlgrs786200881
Max Magnitude0
ClinVar
Risk rs786200881(;)
Alt rs786200881(;)
Reference rs786200881(C;C)
Significance Pathogenic
Disease Atelosteogenesis type 2
Variation info
Gene SLC26A2
CLNDBN Atelosteogenesis type 2
Reversed 0
HGVS NC_000005.9:g.149357606delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000004304.3,