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rs1057520700

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520700(G;T)
Make rs1057520700(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position48685634
GeneWAS
is asnp
is mentioned by
dbSNPrs1057520700
dbSNP (old)rs1057520700
ClinGenrs1057520700
ebirs1057520700
HLIrs1057520700
Exacrs1057520700
Gnomadrs1057520700
Varsomers1057520700
Maprs1057520700
PheGenIrs1057520700
Biobankrs1057520700
1000 genomesrs1057520700
hgdprs1057520700
ensemblrs1057520700
gopubmedrs1057520700
geneviewrs1057520700
scholarrs1057520700
googlers1057520700
pharmgkbrs1057520700
gwascentralrs1057520700
openSNPrs1057520700
23andMers1057520700
23andMe allrs1057520700
SNPshotrs1057520700
SNPdbers1057520700
MSV3drs1057520700
GWAS Ctlgrs1057520700
Max Magnitude0
ClinVar
Risk rs1057520700(A;A) rs1057520700(T;T)
Alt rs1057520700(A;A) rs1057520700(T;T)
Reference Rs1057520700(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WAS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48544023G>A; NC_000023.10:g.48544023G>T
CLNSRC
CLNACC RCV000440734.1, RCV000426711.1,