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rs796053290

From SNPedia

Orientationplus
Geno Mag Summary
(TTTAT;TTTAT) 0 common in clinvar
Make rs796053290(-;-)
Make rs796053290(-;TTTTA)
Make rs796053290(TTTTA;TTTTA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135998099
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053290
ebirs796053290
HLIrs796053290
Exacrs796053290
Varsomers796053290
Maprs796053290
PheGenIrs796053290
hapmaprs796053290
1000 genomesrs796053290
hgdprs796053290
ensemblrs796053290
gopubmedrs796053290
geneviewrs796053290
scholarrs796053290
googlers796053290
pharmgkbrs796053290
gwascentralrs796053290
openSNPrs796053290
23andMers796053290
23andMe allrs796053290
SNP Nexus

SNPshotrs796053290
SNPdbers796053290
MSV3drs796053290
GWAS Ctlgrs796053290
Max Magnitude0
ClinVar
Risk rs796053290(;)
Alt rs796053290(;)
Reference rs796053290(TTTAT;TTTAT)
Significance Pathogenic
Disease not specified Intellectual disability
Variation info
Gene SLC9A6
CLNDBN not specified Intellectual disability
Reversed 0
HGVS NC_000023.10:g.135080258_135080262delTTTTA
CLNSRC
CLNACC RCV000189417.1, RCV000224024.1,