Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524634

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524634(C;C)
Make rs1057524634(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23535146
GeneEARS2
is asnp
is mentioned by
dbSNPrs1057524634
dbSNP (old)rs1057524634
ClinGenrs1057524634
ebirs1057524634
HLIrs1057524634
Exacrs1057524634
Gnomadrs1057524634
Varsomers1057524634
Maprs1057524634
PheGenIrs1057524634
Biobankrs1057524634
1000 genomesrs1057524634
hgdprs1057524634
ensemblrs1057524634
gopubmedrs1057524634
geneviewrs1057524634
scholarrs1057524634
googlers1057524634
pharmgkbrs1057524634
gwascentralrs1057524634
openSNPrs1057524634
23andMers1057524634
23andMe allrs1057524634
SNPshotrs1057524634
SNPdbers1057524634
MSV3drs1057524634
GWAS Ctlgrs1057524634
Max Magnitude0
ClinVar
Risk rs1057524634(C;C)
Alt rs1057524634(C;C)
Reference Rs1057524634(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EARS2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23546467C>G
CLNSRC
CLNACC RCV000441862.1,