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

rs1057520539

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520539(A;A)
Make rs1057520539(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position88545773
GeneKITLG
is asnp
is mentioned by
dbSNPrs1057520539
dbSNP (classic)rs1057520539
ClinGenrs1057520539
ebirs1057520539
HLIrs1057520539
Exacrs1057520539
Gnomadrs1057520539
Varsomers1057520539
LitVarrs1057520539
Maprs1057520539
PheGenIrs1057520539
Biobankrs1057520539
1000 genomesrs1057520539
hgdprs1057520539
ensemblrs1057520539
geneviewrs1057520539
scholarrs1057520539
googlers1057520539
pharmgkbrs1057520539
gwascentralrs1057520539
openSNPrs1057520539
23andMers1057520539
SNPshotrs1057520539
SNPdbers1057520539
MSV3drs1057520539
GWAS Ctlgrs1057520539
Max Magnitude0
ClinVar
Risk rs1057520539(A;A)
Alt rs1057520539(A;A)
Reference Rs1057520539(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KITLG
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.88939550A>T
CLNSRC
CLNACC RCV000445155.1,