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rs137852869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852869(C;C)
Make rs137852869(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position19516253
GeneNDUFA13, TSSK6
is asnp
is mentioned by
dbSNPrs137852869
ebirs137852869
HLIrs137852869
Exacrs137852869
Varsomers137852869
Maprs137852869
PheGenIrs137852869
hapmaprs137852869
1000 genomesrs137852869
hgdprs137852869
ensemblrs137852869
gopubmedrs137852869
geneviewrs137852869
scholarrs137852869
googlers137852869
pharmgkbrs137852869
gwascentralrs137852869
openSNPrs137852869
23andMers137852869
23andMe allrs137852869
SNP Nexus

SNPshotrs137852869
SNPdbers137852869
MSV3drs137852869
GWAS Ctlgrs137852869
Max Magnitude0
OMIM609435
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852869(C;C)
Alt rs137852869(C;C)
Reference rs137852869(G;G)
Significance Pathogenic
Disease Hurthle cell carcinoma of thyroid
Variation info
Gene TSSK6 NDUFA13
CLNDBN Hurthle cell carcinoma of thyroid
Reversed 0
HGVS NC_000019.9:g.19627062G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001761.2,