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rs730880027

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880027(A;A)
Make rs730880027(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219250479
GeneSTK16, TUBA4A
is asnp
is mentioned by
dbSNPrs730880027
ebirs730880027
HLIrs730880027
Exacrs730880027
Varsomers730880027
Maprs730880027
PheGenIrs730880027
hapmaprs730880027
1000 genomesrs730880027
hgdprs730880027
ensemblrs730880027
gopubmedrs730880027
geneviewrs730880027
scholarrs730880027
googlers730880027
pharmgkbrs730880027
gwascentralrs730880027
openSNPrs730880027
23andMers730880027
23andMe allrs730880027
SNP Nexus

SNPshotrs730880027
SNPdbers730880027
MSV3drs730880027
GWAS Ctlgrs730880027
Max Magnitude0
ClinVar
Risk rs730880027(A;A)
Alt rs730880027(A;A)
Reference rs730880027(G;G)
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 1
HGVS NC_000002.11:g.220115201C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157036.3,