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rs1064793164

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position153867993
GeneL1CAM
is asnp
is mentioned by
dbSNPrs1064793164
dbSNP (classic)rs1064793164
ClinGenrs1064793164
ebirs1064793164
HLIrs1064793164
Exacrs1064793164
Gnomadrs1064793164
Varsomers1064793164
LitVarrs1064793164
Maprs1064793164
PheGenIrs1064793164
Biobankrs1064793164
1000 genomesrs1064793164
hgdprs1064793164
ensemblrs1064793164
geneviewrs1064793164
scholarrs1064793164
googlers1064793164
pharmgkbrs1064793164
gwascentralrs1064793164
openSNPrs1064793164
23andMers1064793164
23andMe allrs1064793164
SNPshotrs1064793164
SNPdbers1064793164
MSV3drs1064793164
GWAS Ctlgrs1064793164
Max Magnitude0
ClinVar
Risk rs1064793164(T;T)
Alt rs1064793164(T;T)
Reference Rs1064793164(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene L1CAM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153133448C>A
CLNSRC
CLNACC RCV000480495.1,