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rs1064793292

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
ChromosomeX
Position48688963
is asnp
is mentioned by
dbSNPrs1064793292
dbSNP (classic)rs1064793292
ClinGenrs1064793292
ebirs1064793292
HLIrs1064793292
Exacrs1064793292
Gnomadrs1064793292
Varsomers1064793292
LitVarrs1064793292
Maprs1064793292
PheGenIrs1064793292
Biobankrs1064793292
1000 genomesrs1064793292
hgdprs1064793292
ensemblrs1064793292
geneviewrs1064793292
scholarrs1064793292
googlers1064793292
pharmgkbrs1064793292
gwascentralrs1064793292
openSNPrs1064793292
23andMers1064793292
23andMe allrs1064793292
SNPshotrs1064793292
SNPdbers1064793292
MSV3drs1064793292
GWAS Ctlgrs1064793292
Max Magnitude0
ClinVar
Risk rs1064793292(CCGGGAATGGACCAGCC;CCGGGAATGGACCAGCC)
Alt rs1064793292(CCGGGAATGGACCAGCC;CCGGGAATGGACCAGCC)
Reference Rs1064793292(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48547336_48547352dup17
CLNSRC
CLNACC RCV000479829.1,