Original source

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

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

Chromosome 2:27313032 (forward strand) | View in location tab

Co-located

with COSMIC COSM3391675 (G/A), COSM3391676 (G/A) ; HGMD-PUBLIC CM061856

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_002437.4:c.148C>T, 2178

This variation has 29 HGVS names - click the plus to show

Variation displays