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rs869312932

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312932(G;T)
Make rs869312932(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position100571893
GeneLINS1
is asnp
is mentioned by
dbSNPrs869312932
ebirs869312932
HLIrs869312932
Exacrs869312932
Varsomers869312932
Maprs869312932
PheGenIrs869312932
hapmaprs869312932
1000 genomesrs869312932
hgdprs869312932
ensemblrs869312932
gopubmedrs869312932
geneviewrs869312932
scholarrs869312932
googlers869312932
pharmgkbrs869312932
gwascentralrs869312932
openSNPrs869312932
23andMers869312932
23andMe allrs869312932
SNP Nexus

SNPshotrs869312932
SNPdbers869312932
MSV3drs869312932
GWAS Ctlgrs869312932
Max Magnitude0
ClinVar
Risk rs869312932(T;T)
Alt rs869312932(T;T)
Reference rs869312932(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LINS
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000015.9:g.101112098C>A
CLNSRC
CLNACC RCV000210706.1,