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rs875989951

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs875989951(A;T)
Make rs875989951(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position149978026
GeneSLC26A2
is asnp
is mentioned by
dbSNPrs875989951
ebirs875989951
HLIrs875989951
Exacrs875989951
Varsomers875989951
Maprs875989951
PheGenIrs875989951
hapmaprs875989951
1000 genomesrs875989951
hgdprs875989951
ensemblrs875989951
gopubmedrs875989951
geneviewrs875989951
scholarrs875989951
googlers875989951
pharmgkbrs875989951
gwascentralrs875989951
openSNPrs875989951
23andMers875989951
23andMe allrs875989951
SNP Nexus

SNPshotrs875989951
SNPdbers875989951
MSV3drs875989951
GWAS Ctlgrs875989951
Max Magnitude0
ClinVar
Risk rs875989951(T;T)
Alt rs875989951(T;T)
Reference rs875989951(A;A)
Significance Pathogenic
Disease Atelosteogenesis type 2
Variation info
Gene SLC26A2
CLNDBN Atelosteogenesis type 2
Reversed 0
HGVS NC_000005.9:g.149357589A>T
CLNSRC
CLNACC RCV000211636.1,