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rs767350733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767350733(A;A)
Make rs767350733(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position201724392
GeneALS2
is asnp
is mentioned by
dbSNPrs767350733
dbSNP (classic)rs767350733
ClinGenrs767350733
ebirs767350733
HLIrs767350733
Exacrs767350733
Gnomadrs767350733
Varsomers767350733
LitVarrs767350733
Maprs767350733
PheGenIrs767350733
Biobankrs767350733
1000 genomesrs767350733
hgdprs767350733
ensemblrs767350733
geneviewrs767350733
scholarrs767350733
googlers767350733
pharmgkbrs767350733
gwascentralrs767350733
openSNPrs767350733
23andMers767350733
23andMe allrs767350733
SNPshotrs767350733
SNPdbers767350733
MSV3drs767350733
GWAS Ctlgrs767350733
Max Magnitude0
ClinVar
Risk rs767350733(A;A)
Alt rs767350733(A;A)
Reference Rs767350733(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALS2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.202589115G>A
CLNSRC
CLNACC RCV000421128.1,