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rs1064795049

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position53413227
GeneSMC1A
is asnp
is mentioned by
dbSNPrs1064795049
dbSNP (classic)rs1064795049
ClinGenrs1064795049
ebirs1064795049
HLIrs1064795049
Exacrs1064795049
Gnomadrs1064795049
Varsomers1064795049
LitVarrs1064795049
Maprs1064795049
PheGenIrs1064795049
Biobankrs1064795049
1000 genomesrs1064795049
hgdprs1064795049
ensemblrs1064795049
geneviewrs1064795049
scholarrs1064795049
googlers1064795049
pharmgkbrs1064795049
gwascentralrs1064795049
openSNPrs1064795049
23andMers1064795049
23andMe allrs1064795049
SNPshotrs1064795049
SNPdbers1064795049
MSV3drs1064795049
GWAS Ctlgrs1064795049
Max Magnitude0
ClinVar
Risk rs1064795049(A;A)
Alt rs1064795049(A;A)
Reference Rs1064795049(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMC1A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53440177C>T
CLNSRC
CLNACC RCV000481146.1,