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rs1064793165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome4
Position39473128
GeneLIAS
is asnp
is mentioned by
dbSNPrs1064793165
dbSNP (classic)rs1064793165
ClinGenrs1064793165
ebirs1064793165
HLIrs1064793165
Exacrs1064793165
Gnomadrs1064793165
Varsomers1064793165
LitVarrs1064793165
Maprs1064793165
PheGenIrs1064793165
Biobankrs1064793165
1000 genomesrs1064793165
hgdprs1064793165
ensemblrs1064793165
geneviewrs1064793165
scholarrs1064793165
googlers1064793165
pharmgkbrs1064793165
gwascentralrs1064793165
openSNPrs1064793165
23andMers1064793165
23andMe allrs1064793165
SNPshotrs1064793165
SNPdbers1064793165
MSV3drs1064793165
GWAS Ctlgrs1064793165
Max Magnitude0
ClinVar
Risk rs1064793165(A;A)
Alt rs1064793165(A;A)
Reference Rs1064793165(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LIAS
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.39474748T>A
CLNSRC
CLNACC RCV000478591.1,