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rs112892337

From SNPedia

Orientationplus
Stabilizedplus
Make rs112892337(C;C)
Make rs112892337(C;G)
Make rs112892337(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome8
Position134602310
GeneZFAT
is asnp
is mentioned by
dbSNPrs112892337
dbSNP (old)rs112892337
ClinGenrs112892337
ebirs112892337
HLIrs112892337
Exacrs112892337
Gnomadrs112892337
Varsomers112892337
Maprs112892337
PheGenIrs112892337
Biobankrs112892337
1000 genomesrs112892337
hgdprs112892337
ensemblrs112892337
gopubmedrs112892337
geneviewrs112892337
scholarrs112892337
googlers112892337
pharmgkbrs112892337
gwascentralrs112892337
openSNPrs112892337
23andMers112892337
23andMe allrs112892337
SNPshotrs112892337
SNPdbers112892337
MSV3drs112892337
GWAS Ctlgrs112892337
Max Magnitude

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

ClinVar
Risk rs112892337(C;C)
Alt rs112892337(C;C)
Reference rs112892337(G;G)
Significance Unknown
Disease not specified
Variation info
Gene ZFAT
CLNDBN not specified
Reversed 0
HGVS NC_000008.10:g.135614553G>C
CLNSRC
CLNACC RCV000455390.1,