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rs267606841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606841(G;G)
Make rs267606841(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position165749801
GeneGALNT3
is asnp
is mentioned by
dbSNPrs267606841
ebirs267606841
HLIrs267606841
Exacrs267606841
Varsomers267606841
Maprs267606841
PheGenIrs267606841
hapmaprs267606841
1000 genomesrs267606841
hgdprs267606841
ensemblrs267606841
gopubmedrs267606841
geneviewrs267606841
scholarrs267606841
googlers267606841
pharmgkbrs267606841
gwascentralrs267606841
openSNPrs267606841
23andMers267606841
23andMe allrs267606841
SNP Nexus

SNPshotrs267606841
SNPdbers267606841
MSV3drs267606841
GWAS Ctlgrs267606841
Max Magnitude0
ClinVar
Risk rs267606841(G;G)
Alt rs267606841(G;G)
Reference rs267606841(T;T)
Significance Pathogenic
Disease Tumoral calcinosis
Variation info
Gene GALNT3
CLNDBN Tumoral calcinosis, familial, hyperphosphatemic
Reversed 1
HGVS NC_000002.11:g.166606311A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008246.3,