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rs757966746

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757966746(A;A)
Make rs757966746(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position34294083
GeneAHCY
is asnp
is mentioned by
dbSNPrs757966746
ebirs757966746
HLIrs757966746
Exacrs757966746
Varsomers757966746
Maprs757966746
PheGenIrs757966746
hapmaprs757966746
1000 genomesrs757966746
hgdprs757966746
ensemblrs757966746
gopubmedrs757966746
geneviewrs757966746
scholarrs757966746
googlers757966746
pharmgkbrs757966746
gwascentralrs757966746
openSNPrs757966746
23andMers757966746
23andMe allrs757966746
SNP Nexus

SNPshotrs757966746
SNPdbers757966746
MSV3drs757966746
GWAS Ctlgrs757966746
Max Magnitude0
ClinVar
Risk rs757966746(A;A)
Alt rs757966746(A;A)
Reference rs757966746(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AHCY
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.32881889G>A
CLNSRC
CLNACC RCV000223995.1,