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rs1057518775

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518775(C;G)
Make rs1057518775(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position17387907
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs1057518775
dbSNP (classic)rs1057518775
ClinGenrs1057518775
ebirs1057518775
HLIrs1057518775
Exacrs1057518775
Gnomadrs1057518775
Varsomers1057518775
LitVarrs1057518775
Maprs1057518775
PheGenIrs1057518775
Biobankrs1057518775
1000 genomesrs1057518775
hgdprs1057518775
ensemblrs1057518775
geneviewrs1057518775
scholarrs1057518775
googlers1057518775
pharmgkbrs1057518775
gwascentralrs1057518775
openSNPrs1057518775
23andMers1057518775
SNPshotrs1057518775
SNPdbers1057518775
MSV3drs1057518775
GWAS Ctlgrs1057518775
Max Magnitude0
ClinVar
Risk rs1057518775(G;G)
Alt rs1057518775(G;G)
Reference Rs1057518775(C;C)
Significance Probable-Pathogenic
Disease Atopic dermatitis Hyperinsulinemia Hypertrichosis Hypoglycemia
Variation info
Gene KCNJ11
CLNDBN Atopic dermatitis Hyperinsulinemia Hypertrichosis Hypoglycemia
Reversed 1
HGVS NC_000011.9:g.17409454G>C
CLNSRC
CLNACC RCV000415398.1,