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rs1057523647

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523647(C;T)
Make rs1057523647(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position75971629
GeneTGFB3
is asnp
is mentioned by
dbSNPrs1057523647
dbSNP (old)rs1057523647
ClinGenrs1057523647
ebirs1057523647
HLIrs1057523647
Exacrs1057523647
Gnomadrs1057523647
Varsomers1057523647
Maprs1057523647
PheGenIrs1057523647
Biobankrs1057523647
1000 genomesrs1057523647
hgdprs1057523647
ensemblrs1057523647
gopubmedrs1057523647
geneviewrs1057523647
scholarrs1057523647
googlers1057523647
pharmgkbrs1057523647
gwascentralrs1057523647
openSNPrs1057523647
23andMers1057523647
23andMe allrs1057523647
SNPshotrs1057523647
SNPdbers1057523647
MSV3drs1057523647
GWAS Ctlgrs1057523647
Max Magnitude0
ClinVar
Risk rs1057523647(T;T)
Alt rs1057523647(T;T)
Reference Rs1057523647(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB3
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.76437972G>A
CLNSRC
CLNACC RCV000436458.1,