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rs1057517877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517877(C;T)
Make rs1057517877(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position155730067
GeneGUCY1A3, LOC105377506
is asnp
is mentioned by
dbSNPrs1057517877
dbSNP (classic)rs1057517877
ClinGenrs1057517877
ebirs1057517877
HLIrs1057517877
Exacrs1057517877
Gnomadrs1057517877
Varsomers1057517877
LitVarrs1057517877
Maprs1057517877
PheGenIrs1057517877
Biobankrs1057517877
1000 genomesrs1057517877
hgdprs1057517877
ensemblrs1057517877
geneviewrs1057517877
scholarrs1057517877
googlers1057517877
pharmgkbrs1057517877
gwascentralrs1057517877
openSNPrs1057517877
23andMers1057517877
SNPshotrs1057517877
SNPdbers1057517877
MSV3drs1057517877
GWAS Ctlgrs1057517877
Max Magnitude0
ClinVar
Risk rs1057517877(T;T)
Alt rs1057517877(T;T)
Reference Rs1057517877(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GUCY1A3
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.156651219C>T
CLNSRC
CLNACC RCV000413991.1,