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rs104893657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893657(A;A)
Make rs104893657(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position113246853
GeneC15orf34, PAX8
is asnp
is mentioned by
dbSNPrs104893657
ebirs104893657
HLIrs104893657
Exacrs104893657
Varsomers104893657
Maprs104893657
PheGenIrs104893657
hapmaprs104893657
1000 genomesrs104893657
hgdprs104893657
ensemblrs104893657
gopubmedrs104893657
geneviewrs104893657
scholarrs104893657
googlers104893657
pharmgkbrs104893657
gwascentralrs104893657
openSNPrs104893657
23andMers104893657
23andMe allrs104893657
SNP Nexus

SNPshotrs104893657
SNPdbers104893657
MSV3drs104893657
GWAS Ctlgrs104893657
Max Magnitude0
OMIM167415
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893657(A;A)
Alt rs104893657(A;A)
Reference rs104893657(G;G)
Significance Pathogenic
Disease Thyroid agenesis
Variation info
Gene PAX8 PAX8-AS1
CLNDBN Thyroid agenesis
Reversed 1
HGVS NC_000002.11:g.114004430C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014794.21,