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rs786205577

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205577(A;G)
Make rs786205577(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position10626423
GeneGCNT2
is asnp
is mentioned by
dbSNPrs786205577
ebirs786205577
HLIrs786205577
Exacrs786205577
Varsomers786205577
Maprs786205577
PheGenIrs786205577
hapmaprs786205577
1000 genomesrs786205577
hgdprs786205577
ensemblrs786205577
gopubmedrs786205577
geneviewrs786205577
scholarrs786205577
googlers786205577
pharmgkbrs786205577
gwascentralrs786205577
openSNPrs786205577
23andMers786205577
23andMe allrs786205577
SNP Nexus

SNPshotrs786205577
SNPdbers786205577
MSV3drs786205577
GWAS Ctlgrs786205577
Max Magnitude0
ClinVar
Risk rs786205577(G;G)
Alt rs786205577(G;G)
Reference rs786205577(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCNT2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.10626656A>G
CLNSRC
CLNACC RCV000171391.1,