Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: < 0.01 (T)
Location

Chromosome 1:158655079 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900201, CM910357

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

Variation displays