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rs150591260

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150591260(A;A)
Make rs150591260(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position71641018
GeneMCCC2
is asnp
is mentioned by
dbSNPrs150591260
ebirs150591260
HLIrs150591260
Exacrs150591260
Varsomers150591260
Maprs150591260
PheGenIrs150591260
hapmaprs150591260
1000 genomesrs150591260
hgdprs150591260
ensemblrs150591260
gopubmedrs150591260
geneviewrs150591260
scholarrs150591260
googlers150591260
pharmgkbrs150591260
gwascentralrs150591260
openSNPrs150591260
23andMers150591260
23andMe allrs150591260
SNP Nexus

SNPshotrs150591260
SNPdbers150591260
MSV3drs150591260
GWAS Ctlgrs150591260
Max Magnitude0
ClinVar
Risk rs150591260(A;A)
Alt rs150591260(A;A)
Reference rs150591260(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.70936845G>A
CLNSRC
CLNACC RCV000186002.1,