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rs786205546

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205546(C;C)
Make rs786205546(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position208124230
GeneCRYGD, LOC100507443
is asnp
is mentioned by
dbSNPrs786205546
ebirs786205546
HLIrs786205546
Exacrs786205546
Varsomers786205546
Maprs786205546
PheGenIrs786205546
hapmaprs786205546
1000 genomesrs786205546
hgdprs786205546
ensemblrs786205546
gopubmedrs786205546
geneviewrs786205546
scholarrs786205546
googlers786205546
pharmgkbrs786205546
gwascentralrs786205546
openSNPrs786205546
23andMers786205546
23andMe allrs786205546
SNP Nexus

SNPshotrs786205546
SNPdbers786205546
MSV3drs786205546
GWAS Ctlgrs786205546
Max Magnitude0
ClinVar
Risk rs786205546(C;C)
Alt rs786205546(C;C)
Reference rs786205546(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC100507443 CRYGD
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.208988954A>G
CLNSRC
CLNACC RCV000171329.1,