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rs1057524302

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524302(C;T)
Make rs1057524302(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position196307939
GeneHECW2
is asnp
is mentioned by
dbSNPrs1057524302
dbSNP (old)rs1057524302
ClinGenrs1057524302
ebirs1057524302
HLIrs1057524302
Exacrs1057524302
Gnomadrs1057524302
Varsomers1057524302
Maprs1057524302
PheGenIrs1057524302
Biobankrs1057524302
1000 genomesrs1057524302
hgdprs1057524302
ensemblrs1057524302
gopubmedrs1057524302
geneviewrs1057524302
scholarrs1057524302
googlers1057524302
pharmgkbrs1057524302
gwascentralrs1057524302
openSNPrs1057524302
23andMers1057524302
23andMe allrs1057524302
SNPshotrs1057524302
SNPdbers1057524302
MSV3drs1057524302
GWAS Ctlgrs1057524302
Max Magnitude0
ClinVar
Risk rs1057524302(T;T)
Alt rs1057524302(T;T)
Reference Rs1057524302(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HECW2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.197172663G>A
CLNSRC
CLNACC RCV000425494.1,