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rs137853194

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853194(C;C)
Make rs137853194(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position3225575
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs137853194
ebirs137853194
HLIrs137853194
Exacrs137853194
Varsomers137853194
Maprs137853194
PheGenIrs137853194
hapmaprs137853194
1000 genomesrs137853194
hgdprs137853194
ensemblrs137853194
gopubmedrs137853194
geneviewrs137853194
scholarrs137853194
googlers137853194
pharmgkbrs137853194
gwascentralrs137853194
openSNPrs137853194
23andMers137853194
23andMe allrs137853194
SNP Nexus

SNPshotrs137853194
SNPdbers137853194
MSV3drs137853194
GWAS Ctlgrs137853194
Max Magnitude0
OMIM612850
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853194(C;C)
Alt rs137853194(C;C)
Reference rs137853194(T;T)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene TUBB2B
CLNDBN Polymicrogyria, asymmetric
Reversed 1
HGVS NC_000006.11:g.3225809A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000454.5,