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rs267606727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606727(C;G)
Make rs267606727(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position40471616
GeneCHST14
is asnp
is mentioned by
dbSNPrs267606727
ebirs267606727
HLIrs267606727
Exacrs267606727
Varsomers267606727
Maprs267606727
PheGenIrs267606727
hapmaprs267606727
1000 genomesrs267606727
hgdprs267606727
ensemblrs267606727
gopubmedrs267606727
geneviewrs267606727
scholarrs267606727
googlers267606727
pharmgkbrs267606727
gwascentralrs267606727
openSNPrs267606727
23andMers267606727
23andMe allrs267606727
SNP Nexus

SNPshotrs267606727
SNPdbers267606727
MSV3drs267606727
GWAS Ctlgrs267606727
Max Magnitude0
ClinVar
Risk rs267606727(G;G)
Alt rs267606727(G;G)
Reference rs267606727(C;C)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene CHST14
CLNDBN Ehlers-Danlos syndrome, musculocontractural type
Reversed 0
HGVS NC_000015.9:g.40763815C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002428.4,