Rs104894171

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894171(A;G)
Make rs104894171(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position87508507
GeneMINPP1
is asnp
is mentioned by
dbSNPrs104894171
Exacrs104894171
PheGenIrs104894171
nextbiors104894171
hapmaprs104894171
1000 genomesrs104894171
hgdprs104894171
ensemblrs104894171
gopubmedrs104894171
geneviewrs104894171
scholarrs104894171
googlers104894171
pharmgkbrs104894171
gwascentralrs104894171
openSNPrs104894171
23andMers104894171
23andMe allrs104894171
SNP Nexus

SNPshotrs104894171
SNPdbers104894171
MSV3drs104894171
Max Magnitude0
OMIM605391
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894171(G;G)
Alt rs104894171(G;G)
Reference rs104894171(A;A)
Significance Pathogenic
Disease Thyroid cancer
Variation info
Gene MINPP1
CLNDBN Thyroid cancer, follicular
Reversed 0
HGVS NC_000010.10:g.89268264A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005325.1,