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rs1057524680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524680(C;C)
Make rs1057524680(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position216428638
GeneSMARCAL1
is asnp
is mentioned by
dbSNPrs1057524680
dbSNP (classic)rs1057524680
ClinGenrs1057524680
ebirs1057524680
HLIrs1057524680
Exacrs1057524680
Gnomadrs1057524680
Varsomers1057524680
LitVarrs1057524680
Maprs1057524680
PheGenIrs1057524680
Biobankrs1057524680
1000 genomesrs1057524680
hgdprs1057524680
ensemblrs1057524680
geneviewrs1057524680
scholarrs1057524680
googlers1057524680
pharmgkbrs1057524680
gwascentralrs1057524680
openSNPrs1057524680
23andMers1057524680
23andMe allrs1057524680
SNPshotrs1057524680
SNPdbers1057524680
MSV3drs1057524680
GWAS Ctlgrs1057524680
Max Magnitude0
ClinVar
Risk rs1057524680(C;C)
Alt rs1057524680(C;C)
Reference Rs1057524680(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCAL1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.217293361T>C
CLNSRC
CLNACC RCV000421318.1,