Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064796541

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position153863484
GeneL1CAM
is asnp
is mentioned by
dbSNPrs1064796541
dbSNP (old)rs1064796541
ClinGenrs1064796541
ebirs1064796541
HLIrs1064796541
Exacrs1064796541
Gnomadrs1064796541
Varsomers1064796541
Maprs1064796541
PheGenIrs1064796541
Biobankrs1064796541
1000 genomesrs1064796541
hgdprs1064796541
ensemblrs1064796541
gopubmedrs1064796541
geneviewrs1064796541
scholarrs1064796541
googlers1064796541
pharmgkbrs1064796541
gwascentralrs1064796541
openSNPrs1064796541
23andMers1064796541
23andMe allrs1064796541
SNPshotrs1064796541
SNPdbers1064796541
MSV3drs1064796541
GWAS Ctlgrs1064796541
Max Magnitude0
ClinVar
Risk rs1064796541(A;A)
Alt rs1064796541(A;A)
Reference Rs1064796541(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene L1CAM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153128939C>T
CLNSRC
CLNACC RCV000479930.1,