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rs1064796256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Chromosome1
Position218434147
GeneTGFB2
is asnp
is mentioned by
dbSNPrs1064796256
dbSNP (classic)rs1064796256
ClinGenrs1064796256
ebirs1064796256
HLIrs1064796256
Exacrs1064796256
Gnomadrs1064796256
Varsomers1064796256
LitVarrs1064796256
Maprs1064796256
PheGenIrs1064796256
Biobankrs1064796256
1000 genomesrs1064796256
hgdprs1064796256
ensemblrs1064796256
geneviewrs1064796256
scholarrs1064796256
googlers1064796256
pharmgkbrs1064796256
gwascentralrs1064796256
openSNPrs1064796256
23andMers1064796256
23andMe allrs1064796256
SNPshotrs1064796256
SNPdbers1064796256
MSV3drs1064796256
GWAS Ctlgrs1064796256
Max Magnitude0
ClinVar
Risk rs1064796256(-;-)
Alt rs1064796256(-;-)
Reference Rs1064796256(AA;AA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218607489_218607490delAA
CLNSRC
CLNACC RCV000482233.1,