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rs1057517672

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517672(C;C)
Make rs1057517672(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position91234830
GeneGPR68
is asnp
is mentioned by
dbSNPrs1057517672
dbSNP (old)rs1057517672
ClinGenrs1057517672
ebirs1057517672
HLIrs1057517672
Exacrs1057517672
Gnomadrs1057517672
Varsomers1057517672
Maprs1057517672
PheGenIrs1057517672
Biobankrs1057517672
1000 genomesrs1057517672
hgdprs1057517672
ensemblrs1057517672
gopubmedrs1057517672
geneviewrs1057517672
scholarrs1057517672
googlers1057517672
pharmgkbrs1057517672
gwascentralrs1057517672
openSNPrs1057517672
23andMers1057517672
23andMe allrs1057517672
SNPshotrs1057517672
SNPdbers1057517672
MSV3drs1057517672
GWAS Ctlgrs1057517672
Max Magnitude0
ClinVar
Risk rs1057517672(C;C)
Alt rs1057517672(C;C)
Reference Rs1057517672(T;T)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene GPR68
CLNDBN Amelogenesis imperfecta, hypomaturation type IIA6
Reversed 1
HGVS NC_000014.8:g.91701174A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000412503.1,