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rs754162070

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754162070(G;T)
Make rs754162070(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position1502986
GeneTELO2
is asnp
is mentioned by
dbSNPrs754162070
ebirs754162070
HLIrs754162070
Exacrs754162070
Varsomers754162070
Maprs754162070
PheGenIrs754162070
hapmaprs754162070
1000 genomesrs754162070
hgdprs754162070
ensemblrs754162070
gopubmedrs754162070
geneviewrs754162070
scholarrs754162070
googlers754162070
pharmgkbrs754162070
gwascentralrs754162070
openSNPrs754162070
23andMers754162070
23andMe allrs754162070
SNP Nexus

SNPshotrs754162070
SNPdbers754162070
MSV3drs754162070
GWAS Ctlgrs754162070
Max Magnitude0
ClinVar
Risk rs754162070(T;T)
Alt rs754162070(T;T)
Reference rs754162070(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.1552987G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000225121.2,