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rs1064793853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Chromosome16
Position2048746
GeneNTHL1, TSC2
is asnp
is mentioned by
dbSNPrs1064793853
dbSNP (old)rs1064793853
ClinGenrs1064793853
ebirs1064793853
HLIrs1064793853
Exacrs1064793853
Gnomadrs1064793853
Varsomers1064793853
Maprs1064793853
PheGenIrs1064793853
Biobankrs1064793853
1000 genomesrs1064793853
hgdprs1064793853
ensemblrs1064793853
gopubmedrs1064793853
geneviewrs1064793853
scholarrs1064793853
googlers1064793853
pharmgkbrs1064793853
gwascentralrs1064793853
openSNPrs1064793853
23andMers1064793853
23andMe allrs1064793853
SNPshotrs1064793853
SNPdbers1064793853
MSV3drs1064793853
GWAS Ctlgrs1064793853
Max Magnitude0
ClinVar
Risk rs1064793853(-;-)
Alt rs1064793853(-;-)
Reference Rs1064793853(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene NTHL1 TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2098747_2098748delTA
CLNSRC
CLNACC RCV000481383.1,