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rs398123685

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AACTTCAA;AACTTCAA) 0 common in clinvar
Make rs398123685(-;-)
Make rs398123685(-;AACTTCAA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position120447996
GeneLAMP2
is asnp
is mentioned by
dbSNPrs398123685
ebirs398123685
HLIrs398123685
Exacrs398123685
Varsomers398123685
Maprs398123685
PheGenIrs398123685
hapmaprs398123685
1000 genomesrs398123685
hgdprs398123685
ensemblrs398123685
gopubmedrs398123685
geneviewrs398123685
scholarrs398123685
googlers398123685
pharmgkbrs398123685
gwascentralrs398123685
openSNPrs398123685
23andMers398123685
23andMe allrs398123685
SNP Nexus

SNPshotrs398123685
SNPdbers398123685
MSV3drs398123685
GWAS Ctlgrs398123685
Max Magnitude0
ClinVar
Risk rs398123685(;)
Alt rs398123685(;)
Reference rs398123685(AACTTCAA;AACTTCAA)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119581851_119581858delTTGAAGTT
CLNSRC ClinVar
CLNACC RCV000080004.4,