Have questions? Visit https://www.reddit.com/r/SNPedia

rs71369530

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGCGGC;GGCGGC) 0 common in clinvar
Make rs71369530(-;-)
Make rs71369530(-;GGCGGC)
ReferenceGRCh38 38.1/142
Chromosome9
Position97854446
GeneFOXE1, PTCSC2
is asnp
is mentioned by
dbSNPrs71369530
ebirs71369530
HLIrs71369530
Exacrs71369530
Varsomers71369530
Maprs71369530
PheGenIrs71369530
hapmaprs71369530
1000 genomesrs71369530
hgdprs71369530
ensemblrs71369530
gopubmedrs71369530
geneviewrs71369530
scholarrs71369530
googlers71369530
pharmgkbrs71369530
gwascentralrs71369530
openSNPrs71369530
23andMers71369530
23andMe allrs71369530
SNP Nexus

SNPshotrs71369530
SNPdbers71369530
MSV3drs71369530
GWAS Ctlgrs71369530
Max Magnitude0

[PMID 25879635OA-icon.png] Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population

ClinVar
Risk rs71369530(;)
Alt rs71369530(;)
Reference rs71369530(GGCGGC;GGCGGC)
Significance Non-pathogenic
Disease not specified
Variation info
Gene FOXE1 LOC101928337
CLNDBN not specified
Reversed 1
HGVS NC_000009.11:g.100616728_100616733delGCCGCC
CLNSRC
CLNACC RCV000081102.4,