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rs886039437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039437(A;A)
Make rs886039437(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position169764680
GeneTERC
is asnp
is mentioned by
dbSNPrs886039437
dbSNP (classic)rs886039437
ClinGenrs886039437
ebirs886039437
HLIrs886039437
Exacrs886039437
Gnomadrs886039437
Varsomers886039437
LitVarrs886039437
Maprs886039437
PheGenIrs886039437
Biobankrs886039437
1000 genomesrs886039437
hgdprs886039437
ensemblrs886039437
geneviewrs886039437
scholarrs886039437
googlers886039437
pharmgkbrs886039437
gwascentralrs886039437
openSNPrs886039437
23andMers886039437
23andMe allrs886039437
SNPshotrs886039437
SNPdbers886039437
MSV3drs886039437
GWAS Ctlgrs886039437
Max Magnitude0
ClinVar
Risk rs886039437(A;A)
Alt rs886039437(A;A)
Reference Rs886039437(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TERC
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.169482468C>T
CLNSRC GeneDx
CLNACC RCV000254920.1,