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rs1057520375

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520375(C;G)
Make rs1057520375(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53413132
GeneSMC1A
is asnp
is mentioned by
dbSNPrs1057520375
dbSNP (old)rs1057520375
ClinGenrs1057520375
ebirs1057520375
HLIrs1057520375
Exacrs1057520375
Gnomadrs1057520375
Varsomers1057520375
Maprs1057520375
PheGenIrs1057520375
Biobankrs1057520375
1000 genomesrs1057520375
hgdprs1057520375
ensemblrs1057520375
gopubmedrs1057520375
geneviewrs1057520375
scholarrs1057520375
googlers1057520375
pharmgkbrs1057520375
gwascentralrs1057520375
openSNPrs1057520375
23andMers1057520375
23andMe allrs1057520375
SNPshotrs1057520375
SNPdbers1057520375
MSV3drs1057520375
GWAS Ctlgrs1057520375
Max Magnitude0
ClinVar
Risk rs1057520375(G;G)
Alt rs1057520375(G;G)
Reference Rs1057520375(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMC1A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53440082G>C
CLNSRC
CLNACC RCV000439297.1,