Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:100316614 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960015

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16864, NM_000642.2:c.16C>T

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

Variation displays