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rs1057518558

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518558(G;T)
Make rs1057518558(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position2123805
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs1057518558
dbSNP (old)rs1057518558
ClinGenrs1057518558
ebirs1057518558
HLIrs1057518558
Exacrs1057518558
Gnomadrs1057518558
Varsomers1057518558
LitVarrs1057518558
Maprs1057518558
PheGenIrs1057518558
Biobankrs1057518558
1000 genomesrs1057518558
hgdprs1057518558
ensemblrs1057518558
gopubmedrs1057518558
geneviewrs1057518558
scholarrs1057518558
googlers1057518558
pharmgkbrs1057518558
gwascentralrs1057518558
openSNPrs1057518558
23andMers1057518558
23andMe allrs1057518558
SNPshotrs1057518558
SNPdbers1057518558
MSV3drs1057518558
GWAS Ctlgrs1057518558
Max Magnitude0
ClinVar
Risk rs1057518558(T;T)
Alt rs1057518558(T;T)
Reference Rs1057518558(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCA2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.2123805G>T
CLNSRC
CLNACC RCV000413375.1,