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rs538912281

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs538912281(C;G)
Make rs538912281(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position97854657
GeneFOXE1, PTCSC2
is asnp
is mentioned by
dbSNPrs538912281
ebirs538912281
HLIrs538912281
Exacrs538912281
Varsomers538912281
Maprs538912281
PheGenIrs538912281
hapmaprs538912281
1000 genomesrs538912281
hgdprs538912281
ensemblrs538912281
gopubmedrs538912281
geneviewrs538912281
scholarrs538912281
googlers538912281
pharmgkbrs538912281
gwascentralrs538912281
openSNPrs538912281
23andMers538912281
23andMe allrs538912281
SNP Nexus

SNPshotrs538912281
SNPdbers538912281
MSV3drs538912281
GWAS Ctlgrs538912281
Max Magnitude0
ClinVar
Risk rs538912281(G;G)
Alt rs538912281(G;G)
Reference rs538912281(C;C)
Significance Pathogenic
Disease Thyroid cancer
Variation info
Gene FOXE1 LOC101928337
CLNDBN Thyroid cancer, nonmedullary, 4
Reversed 0
HGVS NC_000009.11:g.100616939C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190467.2,