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rs574376340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs574376340(A;A)
Make rs574376340(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position50168529
GeneLOC105371818, SGCA
is asnp
is mentioned by
dbSNPrs574376340
dbSNP (classic)rs574376340
ClinGenrs574376340
ebirs574376340
HLIrs574376340
Exacrs574376340
Gnomadrs574376340
Varsomers574376340
LitVarrs574376340
Maprs574376340
PheGenIrs574376340
Biobankrs574376340
1000 genomesrs574376340
hgdprs574376340
ensemblrs574376340
geneviewrs574376340
scholarrs574376340
googlers574376340
pharmgkbrs574376340
gwascentralrs574376340
openSNPrs574376340
23andMers574376340
23andMe allrs574376340
SNPshotrs574376340
SNPdbers574376340
MSV3drs574376340
GWAS Ctlgrs574376340
Max Magnitude0
ClinVar
Risk rs574376340(A;A) rs574376340(T;T)
Alt rs574376340(A;A) rs574376340(T;T)
Reference Rs574376340(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene SGCA
CLNDBN not specified not provided
Reversed 0
HGVS NC_000017.10:g.48245890C>A
CLNSRC
CLNACC RCV000377081.1, RCV000486077.1,