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

rs369656775

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369656775(C;T)
Make rs369656775(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position1497457
GeneTELO2
is asnp
is mentioned by
dbSNPrs369656775
ebirs369656775
HLIrs369656775
Exacrs369656775
Varsomers369656775
Maprs369656775
PheGenIrs369656775
hapmaprs369656775
1000 genomesrs369656775
hgdprs369656775
ensemblrs369656775
gopubmedrs369656775
geneviewrs369656775
scholarrs369656775
googlers369656775
pharmgkbrs369656775
gwascentralrs369656775
openSNPrs369656775
23andMers369656775
23andMe allrs369656775
SNP Nexus

SNPshotrs369656775
SNPdbers369656775
MSV3drs369656775
GWAS Ctlgrs369656775
Max Magnitude0
ClinVar
Risk rs369656775(T;T)
Alt rs369656775(T;T)
Reference rs369656775(C;C)
Significance Pathogenic
Disease You-Hoover-Fong syndrome
Variation info
Gene TELO2
CLNDBN You-Hoover-Fong syndrome
Reversed 0
HGVS NC_000016.9:g.1547458C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000225304.2,