Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 10:73539073 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010013

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13244, 11604439

This variation has 3 HGVS names - click the plus to show

10:g.73539073G>A
ENST00000224721.6:c.5252G>A
ENSP00000224721.6:p.Arg1751Gln

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays