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rs150855952

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150855952(A;A)
Make rs150855952(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40418234
GeneIVD
is asnp
is mentioned by
dbSNPrs150855952
dbSNP (old)rs150855952
ClinGenrs150855952
ebirs150855952
HLIrs150855952
Exacrs150855952
Gnomadrs150855952
Varsomers150855952
Maprs150855952
PheGenIrs150855952
Biobankrs150855952
1000 genomesrs150855952
hgdprs150855952
ensemblrs150855952
gopubmedrs150855952
geneviewrs150855952
scholarrs150855952
googlers150855952
pharmgkbrs150855952
gwascentralrs150855952
openSNPrs150855952
23andMers150855952
23andMe allrs150855952
SNP Nexus

SNPshotrs150855952
SNPdbers150855952
MSV3drs150855952
GWAS Ctlgrs150855952
Max Magnitude0
ClinVar
Risk rs150855952(A;A)
Alt rs150855952(A;A)
Reference Rs150855952(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IVD
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40710433G>A
CLNSRC
CLNACC RCV000185978.1,