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rs1057521150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521150(A;A)
Make rs1057521150(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position218436111
GeneTGFB2
is asnp
is mentioned by
dbSNPrs1057521150
dbSNP (classic)rs1057521150
ClinGenrs1057521150
ebirs1057521150
HLIrs1057521150
Exacrs1057521150
Gnomadrs1057521150
Varsomers1057521150
LitVarrs1057521150
Maprs1057521150
PheGenIrs1057521150
Biobankrs1057521150
1000 genomesrs1057521150
hgdprs1057521150
ensemblrs1057521150
geneviewrs1057521150
scholarrs1057521150
googlers1057521150
pharmgkbrs1057521150
gwascentralrs1057521150
openSNPrs1057521150
23andMers1057521150
23andMe allrs1057521150
SNPshotrs1057521150
SNPdbers1057521150
MSV3drs1057521150
GWAS Ctlgrs1057521150
Max Magnitude0
ClinVar
Risk rs1057521150(A;A)
Alt rs1057521150(A;A)
Reference Rs1057521150(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218609453G>A
CLNSRC
CLNACC RCV000418728.1,