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rs146448211

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146448211(A;A)
Make rs146448211(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position36756558
GeneHLCS
is asnp
is mentioned by
dbSNPrs146448211
ebirs146448211
HLIrs146448211
Exacrs146448211
Varsomers146448211
Maprs146448211
PheGenIrs146448211
hapmaprs146448211
1000 genomesrs146448211
hgdprs146448211
ensemblrs146448211
gopubmedrs146448211
geneviewrs146448211
scholarrs146448211
googlers146448211
pharmgkbrs146448211
gwascentralrs146448211
openSNPrs146448211
23andMers146448211
23andMe allrs146448211
SNP Nexus

SNPshotrs146448211
SNPdbers146448211
MSV3drs146448211
GWAS Ctlgrs146448211
Max Magnitude0
ClinVar
Risk rs146448211(A;A)
Alt rs146448211(A;A)
Reference rs146448211(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HLCS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.38128859G>A
CLNSRC
CLNACC RCV000185962.1,