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rs398124181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124181(C;T)
Make rs398124181(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position33381948
GeneLARGE
is asnp
is mentioned by
dbSNPrs398124181
ebirs398124181
HLIrs398124181
Exacrs398124181
Varsomers398124181
Maprs398124181
PheGenIrs398124181
hapmaprs398124181
1000 genomesrs398124181
hgdprs398124181
ensemblrs398124181
gopubmedrs398124181
geneviewrs398124181
scholarrs398124181
googlers398124181
pharmgkbrs398124181
gwascentralrs398124181
openSNPrs398124181
23andMers398124181
23andMe allrs398124181
SNP Nexus

SNPshotrs398124181
SNPdbers398124181
MSV3drs398124181
GWAS Ctlgrs398124181
Max Magnitude0
ClinVar
Risk rs398124181(T;T)
Alt rs398124181(T;T)
Reference rs398124181(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LARGE
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.33777934G>A
CLNSRC ClinVar Emory University
CLNACC RCV000081166.4,