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rs371675497

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371675497(A;A)
Make rs371675497(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position1507605
GeneTELO2
is asnp
is mentioned by
dbSNPrs371675497
ebirs371675497
HLIrs371675497
Exacrs371675497
Varsomers371675497
Maprs371675497
PheGenIrs371675497
hapmaprs371675497
1000 genomesrs371675497
hgdprs371675497
ensemblrs371675497
gopubmedrs371675497
geneviewrs371675497
scholarrs371675497
googlers371675497
pharmgkbrs371675497
gwascentralrs371675497
openSNPrs371675497
23andMers371675497
23andMe allrs371675497
SNP Nexus

SNPshotrs371675497
SNPdbers371675497
MSV3drs371675497
GWAS Ctlgrs371675497
Max Magnitude0
ClinVar
Risk rs371675497(A;A)
Alt rs371675497(A;A)
Reference rs371675497(G;G)
Significance Pathogenic
Disease You-Hoover-Fong syndrome
Variation info
Gene TELO2
CLNDBN You-Hoover-Fong syndrome
Reversed 0
HGVS NC_000016.9:g.1557606G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000225221.2,