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rs1057518230

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518230(A;A)
Make rs1057518230(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2084716
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057518230
dbSNP (old)rs1057518230
ClinGenrs1057518230
ebirs1057518230
HLIrs1057518230
Exacrs1057518230
Gnomadrs1057518230
Varsomers1057518230
Maprs1057518230
PheGenIrs1057518230
Biobankrs1057518230
1000 genomesrs1057518230
hgdprs1057518230
ensemblrs1057518230
gopubmedrs1057518230
geneviewrs1057518230
scholarrs1057518230
googlers1057518230
pharmgkbrs1057518230
gwascentralrs1057518230
openSNPrs1057518230
23andMers1057518230
23andMe allrs1057518230
SNPshotrs1057518230
SNPdbers1057518230
MSV3drs1057518230
GWAS Ctlgrs1057518230
Max Magnitude0
ClinVar
Risk rs1057518230(A;A)
Alt rs1057518230(A;A)
Reference Rs1057518230(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2134717G>A
CLNSRC
CLNACC RCV000412742.2,