Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517895(G;T)
Make rs1057517895(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position49913603
GeneALG12
is asnp
is mentioned by
dbSNPrs1057517895
dbSNP (old)rs1057517895
ClinGenrs1057517895
ebirs1057517895
HLIrs1057517895
Exacrs1057517895
Gnomadrs1057517895
Varsomers1057517895
LitVarrs1057517895
Maprs1057517895
PheGenIrs1057517895
Biobankrs1057517895
1000 genomesrs1057517895
hgdprs1057517895
ensemblrs1057517895
gopubmedrs1057517895
geneviewrs1057517895
scholarrs1057517895
googlers1057517895
pharmgkbrs1057517895
gwascentralrs1057517895
openSNPrs1057517895
23andMers1057517895
23andMe allrs1057517895
SNPshotrs1057517895
SNPdbers1057517895
MSV3drs1057517895
GWAS Ctlgrs1057517895
Max Magnitude0
ClinVar
Risk rs1057517895(T;T)
Alt rs1057517895(T;T)
Reference Rs1057517895(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALG12
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50307251C>A
CLNSRC
CLNACC RCV000414118.1,