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rs797046075

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797046075(A;A)
Make rs797046075(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position3225797
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs797046075
ebirs797046075
HLIrs797046075
Exacrs797046075
Varsomers797046075
Maprs797046075
PheGenIrs797046075
hapmaprs797046075
1000 genomesrs797046075
hgdprs797046075
ensemblrs797046075
gopubmedrs797046075
geneviewrs797046075
scholarrs797046075
googlers797046075
pharmgkbrs797046075
gwascentralrs797046075
openSNPrs797046075
23andMers797046075
23andMe allrs797046075
SNP Nexus

SNPshotrs797046075
SNPdbers797046075
MSV3drs797046075
GWAS Ctlgrs797046075
Max Magnitude0
ClinVar
Risk rs797046075(A;A)
Alt rs797046075(A;A)
Reference rs797046075(G;G)
Significance Probable-Pathogenic
Disease Polymicrogyria
Variation info
Gene TUBB2B
CLNDBN Polymicrogyria, asymmetric
Reversed 1
HGVS NC_000006.11:g.3226031C>T
CLNSRC
CLNACC RCV000192694.1,