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rs797044926

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044926(A;A)
Make rs797044926(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position65523578
GeneLAS1L
is asnp
is mentioned by
dbSNPrs797044926
ebirs797044926
HLIrs797044926
Exacrs797044926
Varsomers797044926
Maprs797044926
PheGenIrs797044926
hapmaprs797044926
1000 genomesrs797044926
hgdprs797044926
ensemblrs797044926
gopubmedrs797044926
geneviewrs797044926
scholarrs797044926
googlers797044926
pharmgkbrs797044926
gwascentralrs797044926
openSNPrs797044926
23andMers797044926
23andMe allrs797044926
SNP Nexus

SNPshotrs797044926
SNPdbers797044926
MSV3drs797044926
GWAS Ctlgrs797044926
Max Magnitude0
ClinVar
Risk rs797044926(A;A)
Alt rs797044926(A;A)
Reference rs797044926(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LAS1L
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.64743458C>T
CLNSRC
CLNACC RCV000190764.1,