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rs750872744

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs750872744(C;T)
Make rs750872744(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position208128325
GeneCRYGC, LOC100507443
is asnp
is mentioned by
dbSNPrs750872744
ebirs750872744
HLIrs750872744
Exacrs750872744
Varsomers750872744
Maprs750872744
PheGenIrs750872744
hapmaprs750872744
1000 genomesrs750872744
hgdprs750872744
ensemblrs750872744
gopubmedrs750872744
geneviewrs750872744
scholarrs750872744
googlers750872744
pharmgkbrs750872744
gwascentralrs750872744
openSNPrs750872744
23andMers750872744
23andMe allrs750872744
SNP Nexus

SNPshotrs750872744
SNPdbers750872744
MSV3drs750872744
GWAS Ctlgrs750872744
Max Magnitude0
ClinVar
Risk rs750872744(T;T)
Alt rs750872744(T;T)
Reference rs750872744(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CRYGC LOC100507443
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.208993049C>A
CLNSRC
CLNACC RCV000171330.1,