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rs730880491

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880491(-;-)
Make rs730880491(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120448990
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880491
ebirs730880491
HLIrs730880491
Exacrs730880491
Varsomers730880491
Maprs730880491
PheGenIrs730880491
hapmaprs730880491
1000 genomesrs730880491
hgdprs730880491
ensemblrs730880491
gopubmedrs730880491
geneviewrs730880491
scholarrs730880491
googlers730880491
pharmgkbrs730880491
gwascentralrs730880491
openSNPrs730880491
23andMers730880491
23andMe allrs730880491
SNP Nexus

SNPshotrs730880491
SNPdbers730880491
MSV3drs730880491
GWAS Ctlgrs730880491
Max Magnitude0
ClinVar
Risk rs730880491(;)
Alt rs730880491(;)
Reference rs730880491(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119582845delT
CLNSRC
CLNACC RCV000157983.1,