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rs200002200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200002200(A;A)
Make rs200002200(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152308777
GeneFLG
is asnp
is mentioned by
dbSNPrs200002200
dbSNP (old)rs200002200
ClinGenrs200002200
ebirs200002200
HLIrs200002200
Exacrs200002200
Gnomadrs200002200
Varsomers200002200
LitVarrs200002200
Maprs200002200
PheGenIrs200002200
Biobankrs200002200
1000 genomesrs200002200
hgdprs200002200
ensemblrs200002200
gopubmedrs200002200
geneviewrs200002200
scholarrs200002200
googlers200002200
pharmgkbrs200002200
gwascentralrs200002200
openSNPrs200002200
23andMers200002200
23andMe allrs200002200
SNPshotrs200002200
SNPdbers200002200
MSV3drs200002200
GWAS Ctlgrs200002200
Max Magnitude0
ClinVar
Risk rs200002200(A;A)
Alt rs200002200(A;A)
Reference Rs200002200(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152281253G>A
CLNSRC
CLNACC RCV000261767.2,