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rs1064795522

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position43192320
GeneHGSNAT
is asnp
is mentioned by
dbSNPrs1064795522
dbSNP (old)rs1064795522
ClinGenrs1064795522
ebirs1064795522
HLIrs1064795522
Exacrs1064795522
Gnomadrs1064795522
Varsomers1064795522
Maprs1064795522
PheGenIrs1064795522
Biobankrs1064795522
1000 genomesrs1064795522
hgdprs1064795522
ensemblrs1064795522
gopubmedrs1064795522
geneviewrs1064795522
scholarrs1064795522
googlers1064795522
pharmgkbrs1064795522
gwascentralrs1064795522
openSNPrs1064795522
23andMers1064795522
23andMe allrs1064795522
SNPshotrs1064795522
SNPdbers1064795522
MSV3drs1064795522
GWAS Ctlgrs1064795522
Max Magnitude0
ClinVar
Risk rs1064795522(T;T)
Alt rs1064795522(T;T)
Reference Rs1064795522(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HGSNAT
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.43047463G>T
CLNSRC
CLNACC RCV000478090.1,