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

rs1057520444

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520444(A;T)
Make rs1057520444(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132897595
GeneTSC1
is asnp
is mentioned by
dbSNPrs1057520444
dbSNP (classic)rs1057520444
ClinGenrs1057520444
ebirs1057520444
HLIrs1057520444
Exacrs1057520444
Gnomadrs1057520444
Varsomers1057520444
LitVarrs1057520444
Maprs1057520444
PheGenIrs1057520444
Biobankrs1057520444
1000 genomesrs1057520444
hgdprs1057520444
ensemblrs1057520444
geneviewrs1057520444
scholarrs1057520444
googlers1057520444
pharmgkbrs1057520444
gwascentralrs1057520444
openSNPrs1057520444
23andMers1057520444
SNPshotrs1057520444
SNPdbers1057520444
MSV3drs1057520444
GWAS Ctlgrs1057520444
Max Magnitude0
ClinVar
Risk rs1057520444(T;T)
Alt rs1057520444(T;T)
Reference Rs1057520444(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135772982T>A
CLNSRC
CLNACC RCV000425755.1,