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rs757520757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757520757(A;A)
Make rs757520757(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position215019784
GeneABCA12
is asnp
is mentioned by
dbSNPrs757520757
dbSNP (classic)rs757520757
ClinGenrs757520757
ebirs757520757
HLIrs757520757
Exacrs757520757
Gnomadrs757520757
Varsomers757520757
LitVarrs757520757
Maprs757520757
PheGenIrs757520757
Biobankrs757520757
1000 genomesrs757520757
hgdprs757520757
ensemblrs757520757
geneviewrs757520757
scholarrs757520757
googlers757520757
pharmgkbrs757520757
gwascentralrs757520757
openSNPrs757520757
23andMers757520757
23andMe allrs757520757
SNPshotrs757520757
SNPdbers757520757
MSV3drs757520757
GWAS Ctlgrs757520757
Max Magnitude0
ClinVar
Risk rs757520757(A;A)
Alt rs757520757(A;A)
Reference Rs757520757(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215884508G>A
CLNSRC
CLNACC RCV000255533.1,