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rs1057518029

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518029(A;G)
Make rs1057518029(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position218434336
GeneTGFB2
is asnp
is mentioned by
dbSNPrs1057518029
dbSNP (old)rs1057518029
ClinGenrs1057518029
ebirs1057518029
HLIrs1057518029
Exacrs1057518029
Gnomadrs1057518029
Varsomers1057518029
Maprs1057518029
PheGenIrs1057518029
Biobankrs1057518029
1000 genomesrs1057518029
hgdprs1057518029
ensemblrs1057518029
gopubmedrs1057518029
geneviewrs1057518029
scholarrs1057518029
googlers1057518029
pharmgkbrs1057518029
gwascentralrs1057518029
openSNPrs1057518029
23andMers1057518029
23andMe allrs1057518029
SNPshotrs1057518029
SNPdbers1057518029
MSV3drs1057518029
GWAS Ctlgrs1057518029
Max Magnitude0
ClinVar
Risk rs1057518029(G;G)
Alt rs1057518029(G;G)
Reference Rs1057518029(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218607678A>G
CLNSRC
CLNACC RCV000413467.1,