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rs45517174

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45517174(A;G)
Make rs45517174(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2064270
GeneTSC2
is asnp
is mentioned by
dbSNPrs45517174
ebirs45517174
HLIrs45517174
Exacrs45517174
Varsomers45517174
Maprs45517174
PheGenIrs45517174
hapmaprs45517174
1000 genomesrs45517174
hgdprs45517174
ensemblrs45517174
gopubmedrs45517174
geneviewrs45517174
scholarrs45517174
googlers45517174
pharmgkbrs45517174
gwascentralrs45517174
openSNPrs45517174
23andMers45517174
23andMe allrs45517174
SNP Nexus

SNPshotrs45517174
SNPdbers45517174
MSV3drs45517174
GWAS Ctlgrs45517174
Max Magnitude0
ClinVar
Risk rs45517174(G;G)
Alt rs45517174(G;G)
Reference rs45517174(A;A)
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.2114271A>G
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042895.2, RCV000201016.1,