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rs742710

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs742710(A;A)
Make rs742710(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position5923382
GeneCHGB
is asnp
is mentioned by
dbSNPrs742710
ebirs742710
HLIrs742710
Exacrs742710
Varsomers742710
Maprs742710
PheGenIrs742710
hapmaprs742710
1000 genomesrs742710
hgdprs742710
ensemblrs742710
gopubmedrs742710
geneviewrs742710
scholarrs742710
googlers742710
pharmgkbrs742710
gwascentralrs742710
openSNPrs742710
23andMers742710
23andMe allrs742710
SNP Nexus

SNPshotrs742710
SNPdbers742710
MSV3drs742710
GWAS Ctlgrs742710
GMAF0.1455
Max Magnitude0
? (A;A) (A;G) (G;G) 28
23andMe blog 2x risk of ALS

[PMID 20007371OA-icon.png] Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.

[PMID 20932227] The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.


GET Evidence
CHGB-P413L
aa_change Pro413Leu
aa_change_short P413L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.108199
summary