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rs1057517671

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057517671(-;-)
Make rs1057517671(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position91234383
GeneGPR68
is asnp
is mentioned by
dbSNPrs1057517671
dbSNP (old)rs1057517671
ClinGenrs1057517671
ebirs1057517671
HLIrs1057517671
Exacrs1057517671
Gnomadrs1057517671
Varsomers1057517671
Maprs1057517671
PheGenIrs1057517671
Biobankrs1057517671
1000 genomesrs1057517671
hgdprs1057517671
ensemblrs1057517671
gopubmedrs1057517671
geneviewrs1057517671
scholarrs1057517671
googlers1057517671
pharmgkbrs1057517671
gwascentralrs1057517671
openSNPrs1057517671
23andMers1057517671
23andMe allrs1057517671
SNPshotrs1057517671
SNPdbers1057517671
MSV3drs1057517671
GWAS Ctlgrs1057517671
Max Magnitude0
ClinVar
Risk rs1057517671(-;-)
Alt rs1057517671(-;-)
Reference Rs1057517671(AA;AA)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene GPR68
CLNDBN Amelogenesis imperfecta, hypomaturation type IIA6
Reversed 1
HGVS NC_000014.8:g.91700727_91700728delTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000412608.1,