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rs797044857

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044857(C;G)
Make rs797044857(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position24354474
GeneGRHL3
is asnp
is mentioned by
dbSNPrs797044857
ebirs797044857
HLIrs797044857
Exacrs797044857
Varsomers797044857
Maprs797044857
PheGenIrs797044857
hapmaprs797044857
1000 genomesrs797044857
hgdprs797044857
ensemblrs797044857
gopubmedrs797044857
geneviewrs797044857
scholarrs797044857
googlers797044857
pharmgkbrs797044857
gwascentralrs797044857
openSNPrs797044857
23andMers797044857
23andMe allrs797044857
SNP Nexus

SNPshotrs797044857
SNPdbers797044857
MSV3drs797044857
GWAS Ctlgrs797044857
Max Magnitude0
ClinVar
Risk rs797044857(G;G)
Alt rs797044857(G;G)
Reference rs797044857(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GRHL3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.24680964C>G
CLNSRC
CLNACC RCV000190659.1,