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rs1057519019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519019(A;A)
Make rs1057519019(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position100573936
GeneLINS1
is asnp
is mentioned by
dbSNPrs1057519019
dbSNP (old)rs1057519019
ClinGenrs1057519019
ebirs1057519019
HLIrs1057519019
Exacrs1057519019
Gnomadrs1057519019
Varsomers1057519019
Maprs1057519019
PheGenIrs1057519019
Biobankrs1057519019
1000 genomesrs1057519019
hgdprs1057519019
ensemblrs1057519019
gopubmedrs1057519019
geneviewrs1057519019
scholarrs1057519019
googlers1057519019
pharmgkbrs1057519019
gwascentralrs1057519019
openSNPrs1057519019
23andMers1057519019
23andMe allrs1057519019
SNPshotrs1057519019
SNPdbers1057519019
MSV3drs1057519019
GWAS Ctlgrs1057519019
Max Magnitude0
ClinVar
Risk rs1057519019(A;A)
Alt rs1057519019(A;A)
Reference Rs1057519019(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene LINS LINS1
CLNDBN Mental retardation, autosomal recessive 27
Reversed 1
HGVS NC_000015.9:g.101114141C>T
CLNSRC
CLNACC RCV000415720.1,