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rs1057524647

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524647(A;T)
Make rs1057524647(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position176727970
GeneVEGFC
is asnp
is mentioned by
dbSNPrs1057524647
dbSNP (old)rs1057524647
ClinGenrs1057524647
ebirs1057524647
HLIrs1057524647
Exacrs1057524647
Gnomadrs1057524647
Varsomers1057524647
Maprs1057524647
PheGenIrs1057524647
Biobankrs1057524647
1000 genomesrs1057524647
hgdprs1057524647
ensemblrs1057524647
gopubmedrs1057524647
geneviewrs1057524647
scholarrs1057524647
googlers1057524647
pharmgkbrs1057524647
gwascentralrs1057524647
openSNPrs1057524647
23andMers1057524647
23andMe allrs1057524647
SNPshotrs1057524647
SNPdbers1057524647
MSV3drs1057524647
GWAS Ctlgrs1057524647
Max Magnitude0
ClinVar
Risk rs1057524647(T;T)
Alt rs1057524647(T;T)
Reference Rs1057524647(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene VEGFC
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.177649124T>A
CLNSRC
CLNACC RCV000417943.1,