Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518633(-;CCACCACC)
Make rs1057518633(CCACCACC;CCACCACC)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position48688918
GeneWAS
is asnp
is mentioned by
dbSNPrs1057518633
dbSNP (old)rs1057518633
ClinGenrs1057518633
ebirs1057518633
HLIrs1057518633
Exacrs1057518633
Gnomadrs1057518633
Varsomers1057518633
LitVarrs1057518633
Maprs1057518633
PheGenIrs1057518633
Biobankrs1057518633
1000 genomesrs1057518633
hgdprs1057518633
ensemblrs1057518633
gopubmedrs1057518633
geneviewrs1057518633
scholarrs1057518633
googlers1057518633
pharmgkbrs1057518633
gwascentralrs1057518633
openSNPrs1057518633
23andMers1057518633
23andMe allrs1057518633
SNPshotrs1057518633
SNPdbers1057518633
MSV3drs1057518633
GWAS Ctlgrs1057518633
Max Magnitude0
ClinVar
Risk rs1057518633(CCACCACC;CCACCACC)
Alt rs1057518633(CCACCACC;CCACCACC)
Reference Rs1057518633(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene WAS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48547300_48547307dupCCACCACC
CLNSRC
CLNACC RCV000414714.1,