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rs45501492

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45501492(A;A)
Make rs45501492(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2079674
GeneTSC2
is asnp
is mentioned by
dbSNPrs45501492
ebirs45501492
HLIrs45501492
Exacrs45501492
Varsomers45501492
Maprs45501492
PheGenIrs45501492
hapmaprs45501492
1000 genomesrs45501492
hgdprs45501492
ensemblrs45501492
gopubmedrs45501492
geneviewrs45501492
scholarrs45501492
googlers45501492
pharmgkbrs45501492
gwascentralrs45501492
openSNPrs45501492
23andMers45501492
23andMe allrs45501492
SNP Nexus

SNPshotrs45501492
SNPdbers45501492
MSV3drs45501492
GWAS Ctlgrs45501492
Max Magnitude0
ClinVar
Risk rs45501492(A,T;A,T)
Alt rs45501492(A,T;A,T)
Reference rs45501492(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.2129675G>A; NC_000016.9:g.2129675G>T
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000043341.2, RCV000190074.1, RCV000055174.1,