Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 6:79916743 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM045143

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_045_ELOVL4_605512_0004, 13233

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

6:g.79916743G>C
ENST00000369816.4:c.810C>G
ENSP00000358831.4:p.Tyr270Ter

Variation displays