Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064794623

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome16
Position83914986
GeneMLYCD
is asnp
is mentioned by
dbSNPrs1064794623
dbSNP (old)rs1064794623
ClinGenrs1064794623
ebirs1064794623
HLIrs1064794623
Exacrs1064794623
Gnomadrs1064794623
Varsomers1064794623
Maprs1064794623
PheGenIrs1064794623
Biobankrs1064794623
1000 genomesrs1064794623
hgdprs1064794623
ensemblrs1064794623
gopubmedrs1064794623
geneviewrs1064794623
scholarrs1064794623
googlers1064794623
pharmgkbrs1064794623
gwascentralrs1064794623
openSNPrs1064794623
23andMers1064794623
23andMe allrs1064794623
SNPshotrs1064794623
SNPdbers1064794623
MSV3drs1064794623
GWAS Ctlgrs1064794623
Max Magnitude0
ClinVar
Risk rs1064794623(C;C)
Alt rs1064794623(C;C)
Reference Rs1064794623(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MLYCD
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.83948591A>C
CLNSRC
CLNACC RCV000487088.1,