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rs1057518414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518414(C;T)
Make rs1057518414(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position2115849
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs1057518414
dbSNP (old)rs1057518414
ClinGenrs1057518414
ebirs1057518414
HLIrs1057518414
Exacrs1057518414
Gnomadrs1057518414
Varsomers1057518414
Maprs1057518414
PheGenIrs1057518414
Biobankrs1057518414
1000 genomesrs1057518414
hgdprs1057518414
ensemblrs1057518414
gopubmedrs1057518414
geneviewrs1057518414
scholarrs1057518414
googlers1057518414
pharmgkbrs1057518414
gwascentralrs1057518414
openSNPrs1057518414
23andMers1057518414
23andMe allrs1057518414
SNPshotrs1057518414
SNPdbers1057518414
MSV3drs1057518414
GWAS Ctlgrs1057518414
Max Magnitude0
ClinVar
Risk rs1057518414(T;T)
Alt rs1057518414(T;T)
Reference Rs1057518414(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMARCA2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.2115849C>T
CLNSRC
CLNACC RCV000414296.1,