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rs1064793632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position7042163
GeneLAMA1
is asnp
is mentioned by
dbSNPrs1064793632
dbSNP (classic)rs1064793632
ClinGenrs1064793632
ebirs1064793632
HLIrs1064793632
Exacrs1064793632
Gnomadrs1064793632
Varsomers1064793632
LitVarrs1064793632
Maprs1064793632
PheGenIrs1064793632
Biobankrs1064793632
1000 genomesrs1064793632
hgdprs1064793632
ensemblrs1064793632
geneviewrs1064793632
scholarrs1064793632
googlers1064793632
pharmgkbrs1064793632
gwascentralrs1064793632
openSNPrs1064793632
23andMers1064793632
23andMe allrs1064793632
SNPshotrs1064793632
SNPdbers1064793632
MSV3drs1064793632
GWAS Ctlgrs1064793632
Max Magnitude0
ClinVar
Risk rs1064793632(-;-)
Alt rs1064793632(-;-)
Reference Rs1064793632(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA1
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.7042162delG
CLNSRC
CLNACC RCV000485226.1,