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rs201637900

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201637900(A;A)
Make rs201637900(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11120424
GeneLDLR
is asnp
is mentioned by
dbSNPrs201637900
ebirs201637900
HLIrs201637900
Exacrs201637900
Varsomers201637900
Maprs201637900
PheGenIrs201637900
hapmaprs201637900
1000 genomesrs201637900
hgdprs201637900
ensemblrs201637900
gopubmedrs201637900
geneviewrs201637900
scholarrs201637900
googlers201637900
pharmgkbrs201637900
gwascentralrs201637900
openSNPrs201637900
23andMers201637900
23andMe allrs201637900
SNP Nexus

SNPshotrs201637900
SNPdbers201637900
MSV3drs201637900
GWAS Ctlgrs201637900
Max Magnitude0
ClinVar
Risk rs201637900(A,C;A,C)
Alt rs201637900(A,C;A,C)
Reference rs201637900(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11231100G>A; NC_000019.9:g.11231100G>C
CLNSRC LDLR @ LOVD
CLNACC RCV000238581.1, RCV000237573.1,