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rs1057518597

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518597(-;-)
Make rs1057518597(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position218405241
GeneTGFB2
is asnp
is mentioned by
dbSNPrs1057518597
dbSNP (old)rs1057518597
ClinGenrs1057518597
ebirs1057518597
HLIrs1057518597
Exacrs1057518597
Gnomadrs1057518597
Varsomers1057518597
LitVarrs1057518597
Maprs1057518597
PheGenIrs1057518597
Biobankrs1057518597
1000 genomesrs1057518597
hgdprs1057518597
ensemblrs1057518597
gopubmedrs1057518597
geneviewrs1057518597
scholarrs1057518597
googlers1057518597
pharmgkbrs1057518597
gwascentralrs1057518597
openSNPrs1057518597
23andMers1057518597
23andMe allrs1057518597
SNPshotrs1057518597
SNPdbers1057518597
MSV3drs1057518597
GWAS Ctlgrs1057518597
Max Magnitude0
ClinVar
Risk rs1057518597(-;-)
Alt rs1057518597(-;-)
Reference Rs1057518597(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218578583delA
CLNSRC
CLNACC RCV000414052.1,