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rs781641023

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781641023(G;T)
Make rs781641023(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position39694633
GeneCOG6
is asnp
is mentioned by
dbSNPrs781641023
ebirs781641023
HLIrs781641023
Exacrs781641023
Varsomers781641023
Maprs781641023
PheGenIrs781641023
hapmaprs781641023
1000 genomesrs781641023
hgdprs781641023
ensemblrs781641023
gopubmedrs781641023
geneviewrs781641023
scholarrs781641023
googlers781641023
pharmgkbrs781641023
gwascentralrs781641023
openSNPrs781641023
23andMers781641023
23andMe allrs781641023
SNP Nexus

SNPshotrs781641023
SNPdbers781641023
MSV3drs781641023
GWAS Ctlgrs781641023
Max Magnitude0
ClinVar
Risk rs781641023(A,T;A,T)
Alt rs781641023(A,T;A,T)
Reference rs781641023(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 2L
Variation info
Gene COG6
CLNDBN Congenital disorder of glycosylation type 2L
Reversed 0
HGVS NC_000013.10:g.40268770G>T
CLNSRC
CLNACC RCV000174392.1,