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rs1064796290

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position144516367
GeneLRRC14, RECQL4
is asnp
is mentioned by
dbSNPrs1064796290
dbSNP (old)rs1064796290
ClinGenrs1064796290
ebirs1064796290
HLIrs1064796290
Exacrs1064796290
Gnomadrs1064796290
Varsomers1064796290
Maprs1064796290
PheGenIrs1064796290
Biobankrs1064796290
1000 genomesrs1064796290
hgdprs1064796290
ensemblrs1064796290
gopubmedrs1064796290
geneviewrs1064796290
scholarrs1064796290
googlers1064796290
pharmgkbrs1064796290
gwascentralrs1064796290
openSNPrs1064796290
23andMers1064796290
23andMe allrs1064796290
SNPshotrs1064796290
SNPdbers1064796290
MSV3drs1064796290
GWAS Ctlgrs1064796290
Max Magnitude0
ClinVar
Risk rs1064796290(-;-)
Alt rs1064796290(-;-)
Reference Rs1064796290(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRRC14 RECQL4
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.145741751delC
CLNSRC
CLNACC RCV000485625.1,