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rs1057518054

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518054(A;A)
Make rs1057518054(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53382327
GeneSMC1A
is asnp
is mentioned by
dbSNPrs1057518054
dbSNP (old)rs1057518054
ClinGenrs1057518054
ebirs1057518054
HLIrs1057518054
Exacrs1057518054
Gnomadrs1057518054
Varsomers1057518054
Maprs1057518054
PheGenIrs1057518054
Biobankrs1057518054
1000 genomesrs1057518054
hgdprs1057518054
ensemblrs1057518054
gopubmedrs1057518054
geneviewrs1057518054
scholarrs1057518054
googlers1057518054
pharmgkbrs1057518054
gwascentralrs1057518054
openSNPrs1057518054
23andMers1057518054
23andMe allrs1057518054
SNPshotrs1057518054
SNPdbers1057518054
MSV3drs1057518054
GWAS Ctlgrs1057518054
Max Magnitude0
ClinVar
Risk rs1057518054(A;A)
Alt rs1057518054(A;A)
Reference Rs1057518054(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMC1A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53409248G>T
CLNSRC
CLNACC RCV000414541.1,