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rs1064797380

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position154379566
GeneEMD
is asnp
is mentioned by
dbSNPrs1064797380
dbSNP (old)rs1064797380
ClinGenrs1064797380
ebirs1064797380
HLIrs1064797380
Exacrs1064797380
Gnomadrs1064797380
Varsomers1064797380
Maprs1064797380
PheGenIrs1064797380
Biobankrs1064797380
1000 genomesrs1064797380
hgdprs1064797380
ensemblrs1064797380
gopubmedrs1064797380
geneviewrs1064797380
scholarrs1064797380
googlers1064797380
pharmgkbrs1064797380
gwascentralrs1064797380
openSNPrs1064797380
23andMers1064797380
23andMe allrs1064797380
SNPshotrs1064797380
SNPdbers1064797380
MSV3drs1064797380
GWAS Ctlgrs1064797380
Max Magnitude0
ClinVar
Risk rs1064797380(A;A)
Alt rs1064797380(A;A)
Reference Rs1064797380(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EMD
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153607926G>A
CLNSRC
CLNACC RCV000487908.1,