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rs35713889

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35713889(C;T)
Make rs35713889(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position49125150
GeneLAMB2
is asnp
is mentioned by
dbSNPrs35713889
dbSNP (old)rs35713889
ClinGenrs35713889
ebirs35713889
HLIrs35713889
Exacrs35713889
Gnomadrs35713889
Varsomers35713889
Maprs35713889
PheGenIrs35713889
Biobankrs35713889
1000 genomesrs35713889
hgdprs35713889
ensemblrs35713889
gopubmedrs35713889
geneviewrs35713889
scholarrs35713889
googlers35713889
pharmgkbrs35713889
gwascentralrs35713889
openSNPrs35713889
23andMers35713889
23andMe allrs35713889
SNP Nexus

SNPshotrs35713889
SNPdbers35713889
MSV3drs35713889
GWAS Ctlgrs35713889
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.
ClinVar
Risk rs35713889(G;G) rs35713889(T;T)
Alt rs35713889(G;G) rs35713889(T;T)
Reference Rs35713889(C;C)
Significance Probable-non-pathogenic
Disease not specified Pierson syndrome Nephrotic syndrome
Variation info
Gene LAMB2
CLNDBN not specified Pierson syndrome Nephrotic syndrome
Reversed 0
HGVS NC_000003.11:g.49162583C>T
CLNSRC
CLNACC RCV000247257.1, RCV000307336.1, RCV000371274.1,