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rs878853099

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853099(A;G)
Make rs878853099(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153869936
GeneL1CAM
is asnp
is mentioned by
dbSNPrs878853099
ebirs878853099
HLIrs878853099
Exacrs878853099
Varsomers878853099
Maprs878853099
PheGenIrs878853099
hapmaprs878853099
1000 genomesrs878853099
hgdprs878853099
ensemblrs878853099
gopubmedrs878853099
geneviewrs878853099
scholarrs878853099
googlers878853099
pharmgkbrs878853099
gwascentralrs878853099
openSNPrs878853099
23andMers878853099
23andMe allrs878853099
SNP Nexus

SNPshotrs878853099
SNPdbers878853099
MSV3drs878853099
GWAS Ctlgrs878853099
Max Magnitude0
ClinVar
Risk rs878853099(G;G)
Alt rs878853099(G;G)
Reference rs878853099(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene L1CAM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153135391T>C
CLNSRC
CLNACC RCV000224561.1,