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rs137853196

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853196(C;C)
Make rs137853196(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position3225296
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs137853196
ebirs137853196
HLIrs137853196
Exacrs137853196
Varsomers137853196
Maprs137853196
PheGenIrs137853196
hapmaprs137853196
1000 genomesrs137853196
hgdprs137853196
ensemblrs137853196
gopubmedrs137853196
geneviewrs137853196
scholarrs137853196
googlers137853196
pharmgkbrs137853196
gwascentralrs137853196
openSNPrs137853196
23andMers137853196
23andMe allrs137853196
SNP Nexus

SNPshotrs137853196
SNPdbers137853196
MSV3drs137853196
GWAS Ctlgrs137853196
Max Magnitude0
OMIM612850
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853196(C;C)
Alt rs137853196(C;C)
Reference rs137853196(T;T)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene TUBB2B
CLNDBN Polymicrogyria, asymmetric
Reversed 1
HGVS NC_000006.11:g.3225530A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000456.4,