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rs730880498

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880498(-;-)
Make rs730880498(-;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120441849
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880498
ebirs730880498
HLIrs730880498
Exacrs730880498
Varsomers730880498
Maprs730880498
PheGenIrs730880498
hapmaprs730880498
1000 genomesrs730880498
hgdprs730880498
ensemblrs730880498
gopubmedrs730880498
geneviewrs730880498
scholarrs730880498
googlers730880498
pharmgkbrs730880498
gwascentralrs730880498
openSNPrs730880498
23andMers730880498
23andMe allrs730880498
SNP Nexus

SNPshotrs730880498
SNPdbers730880498
MSV3drs730880498
GWAS Ctlgrs730880498
Max Magnitude0
ClinVar
Risk rs730880498(;)
Alt rs730880498(;)
Reference rs730880498(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119575704delA
CLNSRC
CLNACC RCV000157991.2,