Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.47 (T)
Location

Chromosome 16:88709737 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR995275

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17701020, rs3189363

This variation has 4 HGVS names - click the plus to show

16:g.88709737C>T
ENST00000261623.3:c.*24G>A
LRG_52:g.12721G>A
LRG_52t1.1:c.*24G>A

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays