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rs1057520655

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520655(A;G)
Make rs1057520655(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position218890257
GeneWNT10A
is asnp
is mentioned by
dbSNPrs1057520655
dbSNP (old)rs1057520655
ClinGenrs1057520655
ebirs1057520655
HLIrs1057520655
Exacrs1057520655
Gnomadrs1057520655
Varsomers1057520655
Maprs1057520655
PheGenIrs1057520655
Biobankrs1057520655
1000 genomesrs1057520655
hgdprs1057520655
ensemblrs1057520655
gopubmedrs1057520655
geneviewrs1057520655
scholarrs1057520655
googlers1057520655
pharmgkbrs1057520655
gwascentralrs1057520655
openSNPrs1057520655
23andMers1057520655
23andMe allrs1057520655
SNPshotrs1057520655
SNPdbers1057520655
MSV3drs1057520655
GWAS Ctlgrs1057520655
Max Magnitude0
ClinVar
Risk rs1057520655(G;G)
Alt rs1057520655(G;G)
Reference Rs1057520655(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene WNT10A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.219754979A>G
CLNSRC
CLNACC RCV000431228.1,