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rs770302956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770302956(C;T)
Make rs770302956(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position209629732
GeneLAMB3
is asnp
is mentioned by
dbSNPrs770302956
dbSNP (classic)rs770302956
ClinGenrs770302956
ebirs770302956
HLIrs770302956
Exacrs770302956
Gnomadrs770302956
Varsomers770302956
LitVarrs770302956
Maprs770302956
PheGenIrs770302956
Biobankrs770302956
1000 genomesrs770302956
hgdprs770302956
ensemblrs770302956
geneviewrs770302956
scholarrs770302956
googlers770302956
pharmgkbrs770302956
gwascentralrs770302956
openSNPrs770302956
23andMers770302956
23andMe allrs770302956
SNPshotrs770302956
SNPdbers770302956
MSV3drs770302956
GWAS Ctlgrs770302956
Max Magnitude0
ClinVar
Risk rs770302956(T;T)
Alt rs770302956(T;T)
Reference Rs770302956(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMB3
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.209803077C>T
CLNSRC
CLNACC RCV000255633.1,