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rs1057518049

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518049(C;T)
Make rs1057518049(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11041349
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1057518049
dbSNP (old)rs1057518049
ClinGenrs1057518049
ebirs1057518049
HLIrs1057518049
Exacrs1057518049
Gnomadrs1057518049
Varsomers1057518049
Maprs1057518049
PheGenIrs1057518049
Biobankrs1057518049
1000 genomesrs1057518049
hgdprs1057518049
ensemblrs1057518049
gopubmedrs1057518049
geneviewrs1057518049
scholarrs1057518049
googlers1057518049
pharmgkbrs1057518049
gwascentralrs1057518049
openSNPrs1057518049
23andMers1057518049
23andMe allrs1057518049
SNPshotrs1057518049
SNPdbers1057518049
MSV3drs1057518049
GWAS Ctlgrs1057518049
Max Magnitude0
ClinVar
Risk rs1057518049(T;T)
Alt rs1057518049(T;T)
Reference Rs1057518049(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCA4
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.11152025C>T
CLNSRC
CLNACC RCV000413081.1,