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rs1057520205

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057520205(-;C)
Make rs1057520205(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position119803378
GeneCIT
is asnp
is mentioned by
dbSNPrs1057520205
dbSNP (classic)rs1057520205
ClinGenrs1057520205
ebirs1057520205
HLIrs1057520205
Exacrs1057520205
Gnomadrs1057520205
Varsomers1057520205
LitVarrs1057520205
Maprs1057520205
PheGenIrs1057520205
Biobankrs1057520205
1000 genomesrs1057520205
hgdprs1057520205
ensemblrs1057520205
geneviewrs1057520205
scholarrs1057520205
googlers1057520205
pharmgkbrs1057520205
gwascentralrs1057520205
openSNPrs1057520205
23andMers1057520205
23andMe allrs1057520205
SNPshotrs1057520205
SNPdbers1057520205
MSV3drs1057520205
GWAS Ctlgrs1057520205
Max Magnitude0
ClinVar
Risk rs1057520205(C;C)
Alt rs1057520205(C;C)
Reference Rs1057520205(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CIT
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.120241183dupG
CLNSRC
CLNACC RCV000431888.1,