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rs1064793438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGCTGCCTG;AGCTGCCTG) 0 common in clinvar
ChromosomeX
Position68838746
GeneEFNB1
is asnp
is mentioned by
dbSNPrs1064793438
dbSNP (classic)rs1064793438
ClinGenrs1064793438
ebirs1064793438
HLIrs1064793438
Exacrs1064793438
Gnomadrs1064793438
Varsomers1064793438
LitVarrs1064793438
Maprs1064793438
PheGenIrs1064793438
Biobankrs1064793438
1000 genomesrs1064793438
hgdprs1064793438
ensemblrs1064793438
geneviewrs1064793438
scholarrs1064793438
googlers1064793438
pharmgkbrs1064793438
gwascentralrs1064793438
openSNPrs1064793438
23andMers1064793438
23andMe allrs1064793438
SNPshotrs1064793438
SNPdbers1064793438
MSV3drs1064793438
GWAS Ctlgrs1064793438
Max Magnitude0
ClinVar
Risk rs1064793438(-;-)
Alt rs1064793438(-;-)
Reference Rs1064793438(AGCTGCCTG;AGCTGCCTG)
Significance Pathogenic
Disease not provided
Variation info
Gene EFNB1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.68058589_68058597delAGCTGCCTG
CLNSRC
CLNACC RCV000487410.1,