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rs1057520333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520333(C;G)
Make rs1057520333(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position43949934
GeneNDP
is asnp
is mentioned by
dbSNPrs1057520333
dbSNP (old)rs1057520333
ClinGenrs1057520333
ebirs1057520333
HLIrs1057520333
Exacrs1057520333
Gnomadrs1057520333
Varsomers1057520333
LitVarrs1057520333
Maprs1057520333
PheGenIrs1057520333
Biobankrs1057520333
1000 genomesrs1057520333
hgdprs1057520333
ensemblrs1057520333
gopubmedrs1057520333
geneviewrs1057520333
scholarrs1057520333
googlers1057520333
pharmgkbrs1057520333
gwascentralrs1057520333
openSNPrs1057520333
23andMers1057520333
23andMe allrs1057520333
SNPshotrs1057520333
SNPdbers1057520333
MSV3drs1057520333
GWAS Ctlgrs1057520333
Max Magnitude0
ClinVar
Risk rs1057520333(G;G)
Alt rs1057520333(G;G)
Reference Rs1057520333(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDP
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.43809180G>C
CLNSRC
CLNACC RCV000440494.1,