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rs765943112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs765943112(G;G)
Make rs765943112(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position23864885
GeneLAMA3
is asnp
is mentioned by
dbSNPrs765943112
dbSNP (classic)rs765943112
ClinGenrs765943112
ebirs765943112
HLIrs765943112
Exacrs765943112
Gnomadrs765943112
Varsomers765943112
LitVarrs765943112
Maprs765943112
PheGenIrs765943112
Biobankrs765943112
1000 genomesrs765943112
hgdprs765943112
ensemblrs765943112
geneviewrs765943112
scholarrs765943112
googlers765943112
pharmgkbrs765943112
gwascentralrs765943112
openSNPrs765943112
23andMers765943112
23andMe allrs765943112
SNPshotrs765943112
SNPdbers765943112
MSV3drs765943112
GWAS Ctlgrs765943112
Max Magnitude0
ClinVar
Risk rs765943112(G;G)
Alt rs765943112(G;G)
Reference Rs765943112(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA3
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.21444849T>G
CLNSRC
CLNACC RCV000443726.1,