Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (T)
Location

Chromosome 1:156849128 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000189 ; PhenCode KinMutBase_NTRK1_DNA:g.19402G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB HSAN4_7

This variation has 18 HGVS names - click the plus to show

Variation displays