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rs1057520786

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520786(A;A)
Make rs1057520786(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position13281099
GenePHYH
is asnp
is mentioned by
dbSNPrs1057520786
dbSNP (old)rs1057520786
ClinGenrs1057520786
ebirs1057520786
HLIrs1057520786
Exacrs1057520786
Gnomadrs1057520786
Varsomers1057520786
LitVarrs1057520786
Maprs1057520786
PheGenIrs1057520786
Biobankrs1057520786
1000 genomesrs1057520786
hgdprs1057520786
ensemblrs1057520786
gopubmedrs1057520786
geneviewrs1057520786
scholarrs1057520786
googlers1057520786
pharmgkbrs1057520786
gwascentralrs1057520786
openSNPrs1057520786
23andMers1057520786
23andMe allrs1057520786
SNPshotrs1057520786
SNPdbers1057520786
MSV3drs1057520786
GWAS Ctlgrs1057520786
Max Magnitude0
ClinVar
Risk rs1057520786(A;A)
Alt rs1057520786(A;A)
Reference Rs1057520786(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PHYH
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.13323099G>T
CLNSRC
CLNACC RCV000443182.1,