Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502827(C;G)
Make rs1060502827(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position75960969
GeneTGFB3
is asnp
is mentioned by
dbSNPrs1060502827
dbSNP (classic)rs1060502827
ClinGenrs1060502827
ebirs1060502827
HLIrs1060502827
Exacrs1060502827
Gnomadrs1060502827
Varsomers1060502827
LitVarrs1060502827
Maprs1060502827
PheGenIrs1060502827
Biobankrs1060502827
1000 genomesrs1060502827
hgdprs1060502827
ensemblrs1060502827
geneviewrs1060502827
scholarrs1060502827
googlers1060502827
pharmgkbrs1060502827
gwascentralrs1060502827
openSNPrs1060502827
23andMers1060502827
SNPshotrs1060502827
SNPdbers1060502827
MSV3drs1060502827
GWAS Ctlgrs1060502827
Max Magnitude0
ClinVar
Risk rs1060502827(G;G)
Alt rs1060502827(G;G)
Reference Rs1060502827(C;C)
Significance Pathogenic
Disease Loeys-Dietz syndrome 4 not provided
Variation info
Gene TGFB3
CLNDBN Loeys-Dietz syndrome 4 not provided
Reversed 1
HGVS NC_000014.8:g.76427312G>C
CLNSRC
CLNACC RCV000472175.1, RCV000482373.1,