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rs201479289

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201479289(A;A)
Make rs201479289(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position49619743
GeneCHAT
is asnp
is mentioned by
dbSNPrs201479289
dbSNP (classic)rs201479289
ClinGenrs201479289
ebirs201479289
HLIrs201479289
Exacrs201479289
Gnomadrs201479289
Varsomers201479289
LitVarrs201479289
Maprs201479289
PheGenIrs201479289
Biobankrs201479289
1000 genomesrs201479289
hgdprs201479289
ensemblrs201479289
geneviewrs201479289
scholarrs201479289
googlers201479289
pharmgkbrs201479289
gwascentralrs201479289
openSNPrs201479289
23andMers201479289
SNPshotrs201479289
SNPdbers201479289
MSV3drs201479289
GWAS Ctlgrs201479289
Max Magnitude0
ClinVar
Risk rs201479289(A;A)
Alt rs201479289(A;A)
Reference Rs201479289(G;G)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene CHAT
CLNDBN not specified not provided
Reversed 0
HGVS NC_000010.10:g.50827789G>A
CLNSRC
CLNACC RCV000260686.1, RCV000331340.1,