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rs45488893

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45488893(A;A)
Make rs45488893(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2056245
GeneTSC2
is asnp
is mentioned by
dbSNPrs45488893
ebirs45488893
HLIrs45488893
Exacrs45488893
Varsomers45488893
Maprs45488893
PheGenIrs45488893
hapmaprs45488893
1000 genomesrs45488893
hgdprs45488893
ensemblrs45488893
gopubmedrs45488893
geneviewrs45488893
scholarrs45488893
googlers45488893
pharmgkbrs45488893
gwascentralrs45488893
openSNPrs45488893
23andMers45488893
23andMe allrs45488893
SNP Nexus

SNPshotrs45488893
SNPdbers45488893
MSV3drs45488893
GWAS Ctlgrs45488893
Max Magnitude0
ClinVar
Risk rs45488893(A;A)
Alt rs45488893(A;A)
Reference rs45488893(G;G)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2106246G>A
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042670.2, RCV000201164.1,