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rs757052602

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757052602(A;T)
Make rs757052602(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position71641068
GeneMCCC2
is asnp
is mentioned by
dbSNPrs757052602
ebirs757052602
HLIrs757052602
Exacrs757052602
Varsomers757052602
Maprs757052602
PheGenIrs757052602
hapmaprs757052602
1000 genomesrs757052602
hgdprs757052602
ensemblrs757052602
gopubmedrs757052602
geneviewrs757052602
scholarrs757052602
googlers757052602
pharmgkbrs757052602
gwascentralrs757052602
openSNPrs757052602
23andMers757052602
23andMe allrs757052602
SNP Nexus

SNPshotrs757052602
SNPdbers757052602
MSV3drs757052602
GWAS Ctlgrs757052602
Max Magnitude0
ClinVar
Risk rs757052602(T;T)
Alt rs757052602(T;T)
Reference rs757052602(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.70936895A>T
CLNSRC
CLNACC RCV000186003.2,