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rs104893659

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893659(A;A)
Make rs104893659(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position113246775
GeneC15orf34, PAX8
is asnp
is mentioned by
dbSNPrs104893659
ebirs104893659
HLIrs104893659
Exacrs104893659
Varsomers104893659
Maprs104893659
PheGenIrs104893659
hapmaprs104893659
1000 genomesrs104893659
hgdprs104893659
ensemblrs104893659
gopubmedrs104893659
geneviewrs104893659
scholarrs104893659
googlers104893659
pharmgkbrs104893659
gwascentralrs104893659
openSNPrs104893659
23andMers104893659
23andMe allrs104893659
SNP Nexus

SNPshotrs104893659
SNPdbers104893659
MSV3drs104893659
GWAS Ctlgrs104893659
Max Magnitude0
OMIM167415
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104893659(A;A)
Alt rs104893659(A;A)
Reference rs104893659(G;G)
Significance Pathogenic
Disease Thyroid agenesis
Variation info
Gene PAX8 PAX8-AS1
CLNDBN Thyroid agenesis
Reversed 1
HGVS NC_000002.11:g.114004352C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014796.25,