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rs1057520757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520757(A;G)
Make rs1057520757(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position100245915
GeneCWF19L1
is asnp
is mentioned by
dbSNPrs1057520757
dbSNP (old)rs1057520757
ClinGenrs1057520757
ebirs1057520757
HLIrs1057520757
Exacrs1057520757
Gnomadrs1057520757
Varsomers1057520757
LitVarrs1057520757
Maprs1057520757
PheGenIrs1057520757
Biobankrs1057520757
1000 genomesrs1057520757
hgdprs1057520757
ensemblrs1057520757
gopubmedrs1057520757
geneviewrs1057520757
scholarrs1057520757
googlers1057520757
pharmgkbrs1057520757
gwascentralrs1057520757
openSNPrs1057520757
23andMers1057520757
23andMe allrs1057520757
SNPshotrs1057520757
SNPdbers1057520757
MSV3drs1057520757
GWAS Ctlgrs1057520757
Max Magnitude0
ClinVar
Risk rs1057520757(G;G)
Alt rs1057520757(G;G)
Reference Rs1057520757(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CWF19L1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.102005672T>C
CLNSRC
CLNACC RCV000421382.1,