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rs119486096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119486096(C;T)
Make rs119486096(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87505037
GeneMINPP1
is asnp
is mentioned by
dbSNPrs119486096
ebirs119486096
HLIrs119486096
Exacrs119486096
Varsomers119486096
Maprs119486096
PheGenIrs119486096
hapmaprs119486096
1000 genomesrs119486096
hgdprs119486096
ensemblrs119486096
gopubmedrs119486096
geneviewrs119486096
scholarrs119486096
googlers119486096
pharmgkbrs119486096
gwascentralrs119486096
openSNPrs119486096
23andMers119486096
23andMe allrs119486096
SNP Nexus

SNPshotrs119486096
SNPdbers119486096
MSV3drs119486096
GWAS Ctlgrs119486096
Max Magnitude0
OMIM605391
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119486096(T;T)
Alt rs119486096(T;T)
Reference rs119486096(C;C)
Significance Pathogenic
Disease Thyroid cancer
Variation info
Gene MINPP1
CLNDBN Thyroid cancer, follicular
Reversed 0
HGVS NC_000010.10:g.89264794C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005324.4,