This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 13:27920235 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM056344

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB IPF1_97C_A_051911

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variant displays