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rs45517150

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45517150(A;A)
Make rs45517150(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2060655
GeneTSC2
is asnp
is mentioned by
dbSNPrs45517150
ebirs45517150
HLIrs45517150
Exacrs45517150
Varsomers45517150
Maprs45517150
PheGenIrs45517150
hapmaprs45517150
1000 genomesrs45517150
hgdprs45517150
ensemblrs45517150
gopubmedrs45517150
geneviewrs45517150
scholarrs45517150
googlers45517150
pharmgkbrs45517150
gwascentralrs45517150
openSNPrs45517150
23andMers45517150
23andMe allrs45517150
SNP Nexus

SNPshotrs45517150
SNPdbers45517150
MSV3drs45517150
GWAS Ctlgrs45517150
Max Magnitude0
ClinVar
Risk rs45517150(A;A)
Alt rs45517150(A;A)
Reference rs45517150(G;G)
Significance Pathogenic
Disease Tuberous sclerosis syndrome not provided
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome not provided
Reversed 0
HGVS NC_000016.9:g.2110656G>A
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042656.2, RCV000189971.1,