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rs62623707

From SNPedia

Orientationplus
Stabilizedplus
Make rs62623707(A;A)
Make rs62623707(A;G)
Make rs62623707(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position135952943
GeneLECT2
is asnp
is mentioned by
dbSNPrs62623707
dbSNP (classic)rs62623707
ClinGenrs62623707
ebirs62623707
HLIrs62623707
Exacrs62623707
Gnomadrs62623707
Varsomers62623707
LitVarrs62623707
Maprs62623707
PheGenIrs62623707
Biobankrs62623707
1000 genomesrs62623707
hgdprs62623707
ensemblrs62623707
geneviewrs62623707
scholarrs62623707
googlers62623707
pharmgkbrs62623707
gwascentralrs62623707
openSNPrs62623707
23andMers62623707
23andMe allrs62623707
SNPshotrs62623707
SNPdbers62623707
MSV3drs62623707
GWAS Ctlgrs62623707
Max Magnitude0

[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.