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rs1064795101

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position17376327
GeneNHS
is asnp
is mentioned by
dbSNPrs1064795101
dbSNP (old)rs1064795101
ClinGenrs1064795101
ebirs1064795101
HLIrs1064795101
Exacrs1064795101
Gnomadrs1064795101
Varsomers1064795101
Maprs1064795101
PheGenIrs1064795101
Biobankrs1064795101
1000 genomesrs1064795101
hgdprs1064795101
ensemblrs1064795101
gopubmedrs1064795101
geneviewrs1064795101
scholarrs1064795101
googlers1064795101
pharmgkbrs1064795101
gwascentralrs1064795101
openSNPrs1064795101
23andMers1064795101
23andMe allrs1064795101
SNPshotrs1064795101
SNPdbers1064795101
MSV3drs1064795101
GWAS Ctlgrs1064795101
Max Magnitude0
ClinVar
Risk rs1064795101(A;A)
Alt rs1064795101(A;A)
Reference Rs1064795101(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NHS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.17394450G>A
CLNSRC
CLNACC RCV000483234.1,