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rs587776893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776893(-;-)
Make rs587776893(-;AC)
Make rs587776893(AC;AC)
ReferenceGRCh38 38.1/142
Chromosome8
Position37753522
GeneERLIN2
is asnp
is mentioned by
dbSNPrs587776893
ebirs587776893
HLIrs587776893
Exacrs587776893
Varsomers587776893
Maprs587776893
PheGenIrs587776893
hapmaprs587776893
1000 genomesrs587776893
hgdprs587776893
ensemblrs587776893
gopubmedrs587776893
geneviewrs587776893
scholarrs587776893
googlers587776893
pharmgkbrs587776893
gwascentralrs587776893
openSNPrs587776893
23andMers587776893
23andMe allrs587776893
SNP Nexus

SNPshotrs587776893
SNPdbers587776893
MSV3drs587776893
GWAS Ctlgrs587776893
Max Magnitude0
ClinVar
Risk rs587776893(CA;CA)
Alt rs587776893(CA;CA)
Reference rs587776893(;)
Significance Pathogenic
Disease Spastic paraplegia 18
Variation info
Gene ERLIN2
CLNDBN Spastic paraplegia 18
Reversed 0
HGVS NC_000008.10:g.37611040_37611041insAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000023901.4,