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rs1057517941

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517941(C;T)
Make rs1057517941(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position38299386
GeneSPRED1
is asnp
is mentioned by
dbSNPrs1057517941
dbSNP (old)rs1057517941
ClinGenrs1057517941
ebirs1057517941
HLIrs1057517941
Exacrs1057517941
Gnomadrs1057517941
Varsomers1057517941
Maprs1057517941
PheGenIrs1057517941
Biobankrs1057517941
1000 genomesrs1057517941
hgdprs1057517941
ensemblrs1057517941
gopubmedrs1057517941
geneviewrs1057517941
scholarrs1057517941
googlers1057517941
pharmgkbrs1057517941
gwascentralrs1057517941
openSNPrs1057517941
23andMers1057517941
23andMe allrs1057517941
SNPshotrs1057517941
SNPdbers1057517941
MSV3drs1057517941
GWAS Ctlgrs1057517941
Max Magnitude0
ClinVar
Risk rs1057517941(T;T)
Alt rs1057517941(T;T)
Reference Rs1057517941(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SPRED1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.38591587C>T
CLNSRC
CLNACC RCV000414009.1,