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rs1057523129

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523129(C;C)
Make rs1057523129(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position146124014
GeneLARS
is asnp
is mentioned by
dbSNPrs1057523129
dbSNP (old)rs1057523129
ClinGenrs1057523129
ebirs1057523129
HLIrs1057523129
Exacrs1057523129
Gnomadrs1057523129
Varsomers1057523129
Maprs1057523129
PheGenIrs1057523129
Biobankrs1057523129
1000 genomesrs1057523129
hgdprs1057523129
ensemblrs1057523129
gopubmedrs1057523129
geneviewrs1057523129
scholarrs1057523129
googlers1057523129
pharmgkbrs1057523129
gwascentralrs1057523129
openSNPrs1057523129
23andMers1057523129
23andMe allrs1057523129
SNPshotrs1057523129
SNPdbers1057523129
MSV3drs1057523129
GWAS Ctlgrs1057523129
Max Magnitude0
ClinVar
Risk rs1057523129(C;C)
Alt rs1057523129(C;C)
Reference Rs1057523129(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LARS
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.145503577C>G
CLNSRC
CLNACC RCV000443951.1,