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

rs797044940

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044940(C;C)
Make rs797044940(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position6958571
GeneLAMA1
is asnp
is mentioned by
dbSNPrs797044940
ebirs797044940
HLIrs797044940
Exacrs797044940
Varsomers797044940
Maprs797044940
PheGenIrs797044940
hapmaprs797044940
1000 genomesrs797044940
hgdprs797044940
ensemblrs797044940
gopubmedrs797044940
geneviewrs797044940
scholarrs797044940
googlers797044940
pharmgkbrs797044940
gwascentralrs797044940
openSNPrs797044940
23andMers797044940
23andMe allrs797044940
SNP Nexus

SNPshotrs797044940
SNPdbers797044940
MSV3drs797044940
GWAS Ctlgrs797044940
Max Magnitude0
ClinVar
Risk rs797044940(C;C)
Alt rs797044940(C;C)
Reference rs797044940(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LAMA1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000018.9:g.6958570A>G
CLNSRC
CLNACC RCV000190786.1,