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rs376664522

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376664522(A;A)
Make rs376664522(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position219212413
GeneABCB6
is asnp
is mentioned by
dbSNPrs376664522
dbSNP (classic)rs376664522
ClinGenrs376664522
ebirs376664522
HLIrs376664522
Exacrs376664522
Gnomadrs376664522
Varsomers376664522
LitVarrs376664522
Maprs376664522
PheGenIrs376664522
Biobankrs376664522
1000 genomesrs376664522
hgdprs376664522
ensemblrs376664522
geneviewrs376664522
scholarrs376664522
googlers376664522
pharmgkbrs376664522
gwascentralrs376664522
openSNPrs376664522
23andMers376664522
SNPshotrs376664522
SNPdbers376664522
MSV3drs376664522
GWAS Ctlgrs376664522
Max Magnitude0
ClinVar
Risk rs376664522(A;A)
Alt rs376664522(A;A)
Reference Rs376664522(G;G)
Significance Other
Disease Langereis blood group
Variation info
Gene ABCB6
CLNDBN Langereis blood group
Reversed 0
HGVS NC_000002.11:g.220077135G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023436.3,