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rs1057518095

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518095(C;C)
Make rs1057518095(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position40819462
GeneKCNQ4
is asnp
is mentioned by
dbSNPrs1057518095
dbSNP (old)rs1057518095
ClinGenrs1057518095
ebirs1057518095
HLIrs1057518095
Exacrs1057518095
Gnomadrs1057518095
Varsomers1057518095
Maprs1057518095
PheGenIrs1057518095
Biobankrs1057518095
1000 genomesrs1057518095
hgdprs1057518095
ensemblrs1057518095
gopubmedrs1057518095
geneviewrs1057518095
scholarrs1057518095
googlers1057518095
pharmgkbrs1057518095
gwascentralrs1057518095
openSNPrs1057518095
23andMers1057518095
23andMe allrs1057518095
SNPshotrs1057518095
SNPdbers1057518095
MSV3drs1057518095
GWAS Ctlgrs1057518095
Max Magnitude0
ClinVar
Risk rs1057518095(C;C)
Alt rs1057518095(C;C)
Reference Rs1057518095(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ4
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.41285134G>C
CLNSRC
CLNACC RCV000412910.1,