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rs748363752

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs748363752(A;G)
Make rs748363752(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position49431819
GeneMUT
is asnp
is mentioned by
dbSNPrs748363752
ebirs748363752
HLIrs748363752
Exacrs748363752
Varsomers748363752
Maprs748363752
PheGenIrs748363752
hapmaprs748363752
1000 genomesrs748363752
hgdprs748363752
ensemblrs748363752
gopubmedrs748363752
geneviewrs748363752
scholarrs748363752
googlers748363752
pharmgkbrs748363752
gwascentralrs748363752
openSNPrs748363752
23andMers748363752
23andMe allrs748363752
SNP Nexus

SNPshotrs748363752
SNPdbers748363752
MSV3drs748363752
GWAS Ctlgrs748363752
Max Magnitude0
ClinVar
Risk rs748363752(G;G)
Alt rs748363752(G;G)
Reference rs748363752(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.49399532A>T
CLNSRC
CLNACC RCV000186052.1,