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rs768913919

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768913919(C;T)
Make rs768913919(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position158111415
GeneSERAC1
is asnp
is mentioned by
dbSNPrs768913919
ebirs768913919
HLIrs768913919
Exacrs768913919
Varsomers768913919
Maprs768913919
PheGenIrs768913919
hapmaprs768913919
1000 genomesrs768913919
hgdprs768913919
ensemblrs768913919
gopubmedrs768913919
geneviewrs768913919
scholarrs768913919
googlers768913919
pharmgkbrs768913919
gwascentralrs768913919
openSNPrs768913919
23andMers768913919
23andMe allrs768913919
SNP Nexus

SNPshotrs768913919
SNPdbers768913919
MSV3drs768913919
GWAS Ctlgrs768913919
Max Magnitude0
ClinVar
Risk rs768913919(T;T)
Alt rs768913919(T;T)
Reference rs768913919(C;C)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene SERAC1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000006.11:g.158532447C>G; NC_000006.11:g.158532447C>T
CLNSRC
CLNACC RCV000197976.2, RCV000195730.1,