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rs368743618

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368743618(C;T)
Make rs368743618(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219250552
GeneSTK16, TUBA4A
is asnp
is mentioned by
dbSNPrs368743618
ebirs368743618
HLIrs368743618
Exacrs368743618
Varsomers368743618
Maprs368743618
PheGenIrs368743618
hapmaprs368743618
1000 genomesrs368743618
hgdprs368743618
ensemblrs368743618
gopubmedrs368743618
geneviewrs368743618
scholarrs368743618
googlers368743618
pharmgkbrs368743618
gwascentralrs368743618
openSNPrs368743618
23andMers368743618
23andMe allrs368743618
SNP Nexus

SNPshotrs368743618
SNPdbers368743618
MSV3drs368743618
GWAS Ctlgrs368743618
Max Magnitude0
ClinVar
Risk rs368743618(T;T)
Alt rs368743618(T;T)
Reference rs368743618(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia
Variation info
Gene STK16 TUBA4A
CLNDBN Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia
Reversed 0
HGVS NC_000002.11:g.220115274C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157038.3,