Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 16:88810550 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910042

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_008_APRT_102600_0004, 87, NM_000485.2:c.194A>T

This variation has 13 HGVS names - click the plus to show

Variation displays