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

rs754323928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754323928(C;G)
Make rs754323928(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position23876394
GeneLAMA3
is asnp
is mentioned by
dbSNPrs754323928
dbSNP (classic)rs754323928
ClinGenrs754323928
ebirs754323928
HLIrs754323928
Exacrs754323928
Gnomadrs754323928
Varsomers754323928
LitVarrs754323928
Maprs754323928
PheGenIrs754323928
Biobankrs754323928
1000 genomesrs754323928
hgdprs754323928
ensemblrs754323928
geneviewrs754323928
scholarrs754323928
googlers754323928
pharmgkbrs754323928
gwascentralrs754323928
openSNPrs754323928
23andMers754323928
23andMe allrs754323928
SNPshotrs754323928
SNPdbers754323928
MSV3drs754323928
GWAS Ctlgrs754323928
Max Magnitude0
ClinVar
Risk rs754323928(G;G)
Alt rs754323928(G;G)
Reference Rs754323928(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA3
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.21456358C>G
CLNSRC
CLNACC RCV000484655.1,