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rs35658696

From SNPedia

Orientationminus
Stabilizedminus
Make rs35658696(C;C)
Make rs35658696(C;T)
Make rs35658696(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position103003107
GenePAM
is asnp
is mentioned by
dbSNPrs35658696
dbSNP (classic)rs35658696
ClinGenrs35658696
ebirs35658696
HLIrs35658696
Exacrs35658696
Gnomadrs35658696
Varsomers35658696
LitVarrs35658696
Maprs35658696
PheGenIrs35658696
Biobankrs35658696
1000 genomesrs35658696
hgdprs35658696
ensemblrs35658696
geneviewrs35658696
scholarrs35658696
googlers35658696
pharmgkbrs35658696
gwascentralrs35658696
openSNPrs35658696
23andMers35658696
23andMe allrs35658696
SNPshotrs35658696
SNPdbers35658696
MSV3drs35658696
GWAS Ctlgrs35658696
Max Magnitude0

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