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rs527236214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATTT;ATTT) 0 common in clinvar
Make rs527236214(-;-)
Make rs527236214(-;ATTT)
ReferenceGRCh38 38.1/142
Chromosome1
Position231487317
is asnp
is mentioned by
dbSNPrs527236214
ebirs527236214
HLIrs527236214
Exacrs527236214
Varsomers527236214
Maprs527236214
PheGenIrs527236214
hapmaprs527236214
1000 genomesrs527236214
hgdprs527236214
ensemblrs527236214
gopubmedrs527236214
geneviewrs527236214
scholarrs527236214
googlers527236214
pharmgkbrs527236214
gwascentralrs527236214
openSNPrs527236214
23andMers527236214
23andMe allrs527236214
SNP Nexus

SNPshotrs527236214
SNPdbers527236214
MSV3drs527236214
GWAS Ctlgrs527236214
Max Magnitude0
ClinVar
Risk rs527236214(;)
Alt rs527236214(;)
Reference rs527236214(ATTT;ATTT)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724041
CLNDBN not provided
Reversed 0
HGVS NC_000001.11:g.231487317_231487320delATTT
CLNSRC
CLNACC RCV000133470.1,