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rs1057523765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523765(A;G)
Make rs1057523765(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position135031510
GeneC5orf66, PITX1
is asnp
is mentioned by
dbSNPrs1057523765
dbSNP (classic)rs1057523765
ClinGenrs1057523765
ebirs1057523765
HLIrs1057523765
Exacrs1057523765
Gnomadrs1057523765
Varsomers1057523765
LitVarrs1057523765
Maprs1057523765
PheGenIrs1057523765
Biobankrs1057523765
1000 genomesrs1057523765
hgdprs1057523765
ensemblrs1057523765
geneviewrs1057523765
scholarrs1057523765
googlers1057523765
pharmgkbrs1057523765
gwascentralrs1057523765
openSNPrs1057523765
23andMers1057523765
SNPshotrs1057523765
SNPdbers1057523765
MSV3drs1057523765
GWAS Ctlgrs1057523765
Max Magnitude0
ClinVar
Risk rs1057523765(G;G)
Alt rs1057523765(G;G)
Reference Rs1057523765(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C5orf66 PITX1
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.134367200T>C
CLNSRC
CLNACC RCV000437266.1,