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rs1057520784

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520784(A;G)
Make rs1057520784(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position2110407
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs1057520784
dbSNP (old)rs1057520784
ClinGenrs1057520784
ebirs1057520784
HLIrs1057520784
Exacrs1057520784
Gnomadrs1057520784
Varsomers1057520784
Maprs1057520784
PheGenIrs1057520784
Biobankrs1057520784
1000 genomesrs1057520784
hgdprs1057520784
ensemblrs1057520784
gopubmedrs1057520784
geneviewrs1057520784
scholarrs1057520784
googlers1057520784
pharmgkbrs1057520784
gwascentralrs1057520784
openSNPrs1057520784
23andMers1057520784
23andMe allrs1057520784
SNPshotrs1057520784
SNPdbers1057520784
MSV3drs1057520784
GWAS Ctlgrs1057520784
Max Magnitude0
ClinVar
Risk rs1057520784(G;G)
Alt rs1057520784(G;G)
Reference Rs1057520784(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SMARCA2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.2110407A>G
CLNSRC
CLNACC RCV000431579.1,