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rs1057523836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523836(A;A)
Make rs1057523836(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position2110347
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs1057523836
dbSNP (old)rs1057523836
ClinGenrs1057523836
ebirs1057523836
HLIrs1057523836
Exacrs1057523836
Gnomadrs1057523836
Varsomers1057523836
Maprs1057523836
PheGenIrs1057523836
Biobankrs1057523836
1000 genomesrs1057523836
hgdprs1057523836
ensemblrs1057523836
gopubmedrs1057523836
geneviewrs1057523836
scholarrs1057523836
googlers1057523836
pharmgkbrs1057523836
gwascentralrs1057523836
openSNPrs1057523836
23andMers1057523836
23andMe allrs1057523836
SNPshotrs1057523836
SNPdbers1057523836
MSV3drs1057523836
GWAS Ctlgrs1057523836
Max Magnitude0
ClinVar
Risk rs1057523836(A;A)
Alt rs1057523836(A;A)
Reference Rs1057523836(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCA2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.2110347G>A
CLNSRC
CLNACC RCV000442641.1,