Original source

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

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

Chromosome 5:1264541 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM054141

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5548, NM_198253.2:c.2706G>C

This variation has 10 HGVS names - click the plus to show

Variation displays