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rs1064797348

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position101573734
GeneGRHL2
is asnp
is mentioned by
dbSNPrs1064797348
dbSNP (old)rs1064797348
ClinGenrs1064797348
ebirs1064797348
HLIrs1064797348
Exacrs1064797348
Gnomadrs1064797348
Varsomers1064797348
Maprs1064797348
PheGenIrs1064797348
Biobankrs1064797348
1000 genomesrs1064797348
hgdprs1064797348
ensemblrs1064797348
gopubmedrs1064797348
geneviewrs1064797348
scholarrs1064797348
googlers1064797348
pharmgkbrs1064797348
gwascentralrs1064797348
openSNPrs1064797348
23andMers1064797348
23andMe allrs1064797348
SNPshotrs1064797348
SNPdbers1064797348
MSV3drs1064797348
GWAS Ctlgrs1064797348
Max Magnitude0
ClinVar
Risk rs1064797348(-;-)
Alt rs1064797348(-;-)
Reference Rs1064797348(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRHL2
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.102585962delG
CLNSRC
CLNACC RCV000487664.1,